U.S. flag

An official website of the United States government

NCBI Bookshelf. A service of the National Library of Medicine, National Institutes of Health.

Adam MP, Feldman J, Mirzaa GM, et al., editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2024.

Cover of GeneReviews®

GeneReviews® [Internet].

Show details

Lowe Syndrome

Synonyms: Oculocerebrorenal Syndrome, Oculocerebrorenal Syndrome of Lowe

, MD, MS, , MD, and , MD.

Author Information and Affiliations

Initial Posting: ; Last Update: April 18, 2019.

Estimated reading time: 30 minutes

Summary

Clinical characteristics.

Lowe syndrome (oculocerebrorenal syndrome) is characterized by involvement of the eyes, central nervous system, and kidneys. Dense congenital cataracts are found in all affected boys and infantile glaucoma in approximately 50%. All boys have impaired vision; corrected acuity is rarely better than 20/100. Generalized hypotonia is noted at birth and is of central (brain) origin. Deep tendon reflexes are usually absent. Hypotonia may slowly improve with age, but normal motor tone and strength are never achieved. Motor milestones are delayed. Almost all affected males have some degree of intellectual disability; 10%-25% function in the low-normal or borderline range, approximately 25% in the mild-to-moderate range, and 50%-65% in the severe-to-profound range of intellectual disability. Affected males have varying degrees of proximal renal tubular dysfunction of the Fanconi type, including low molecular-weight (LMW) proteinuria, aminoaciduria, bicarbonate wasting and renal tubular acidosis, phosphaturia with hypophosphatemia and renal rickets, hypercalciuria, sodium and potassium wasting, and polyuria. The features of symptomatic Fanconi syndrome do not usually become manifest until after the first few months of life, except for LMW proteinuria. Glomerulosclerosis associated with chronic tubular injury usually results in slowly progressive chronic renal failure and end-stage renal disease between the second and fourth decades of life.

Diagnosis/testing.

The diagnosis of Lowe syndrome is established in a male proband with typical clinical and laboratory findings and a hemizygous pathogenic variant in OCRL identified by molecular genetic testing. The diagnosis of Lowe syndrome is rare in females but can be established in a female proband who demonstrates the same clinical and laboratory findings as a male proband and who is found to have a heterozygous pathogenic variant in OCRL by molecular genetic testing.

Management.

Treatment of manifestations:

  • Early removal of cataracts with postoperative glasses; management of glaucoma; early infant therapy, preschool intervention program and individualized education program throughout schooling; behavior modification plan; anticonvulsant therapy if seizures are present.
  • Treatment of renal tubular dysfunction includes oral supplements of sodium and potassium bicarbonate or citrate to correct acidosis and hypokalemia, and oral phosphate and oral calcitriol (1,25-dihydroxyvitamin D3) to correct hypophosphatemia and renal rickets; treatment of ESRD with chronic dialysis and renal transplant in selected individuals.
  • Consider human growth hormone therapy to improve growth velocity; tube feedings may be needed to treat infant feeding problems associated with hypotonia; standard treatment for gastroesophageal reflux if present. Bracing or surgery for severe or progressive scoliosis or joint hypermobility; resection of fibromas and cutaneous cysts if painful or impairing function.

Surveillance: Intraocular pressure monitoring every six months for life, other eye evaluations at intervals determined by specialist; at least annual assessment of kidney function, growth, developmental progress; annual evaluation for scoliosis and joint problems; semiannual dental examinations.

Circumstances to avoid: Corneal contact lenses because of associated risk of corneal keloid formation and complexities of contact lens care; artificial lens implants because of probable increased risk of glaucoma.

Genetic counseling.

Lowe syndrome is inherited in an X-linked manner. De novo pathogenic variants have been reported in 32% of males affected with Lowe syndrome. A high risk of germline mosaicism (4.5%) has been identified. When a mother is a heterozygous, each pregnancy has a 25% chance of an affected son, a 25% chance of a heterozygous daughter, a 25% chance of an unaffected son, and a 25% chance of a daughter who is not heterozygous. No affected male is known to have reproduced. Approximately 95% of heterozygous females older than age 15 years have characteristic findings in the lens of the eye on slit lamp examination by an experienced ophthalmologist using both direct and retroillumination. Once the OCRL pathogenic variant has been identified in an affected family member, prenatal and preimplantation genetic testing are possible.

Diagnosis

Suggestive Findings

Lowe syndrome should be suspected in a proband with a combination of the following features:

  • Bilateral dense congenital cataracts
  • Infantile congenital hypotonia
  • Delayed development
  • Proximal renal tubular transport dysfunction of the Fanconi type characterized by low molecular-weight (LMW) proteinuria (including retinol binding protein, N-acetyl glucosaminidase, and albumin), aminoaciduria and varying degrees of bicarbonaturia and acidosis, phosphaturia and hypophosphatemia, and hypercalciuria.

Note: LMW proteinuria, characterized by the excretion of proteins such as retinal binding protein and N-acetyl glucosaminidase, is seen in Lowe syndrome, the allelic disorder Dent disease (see Genetically Related Disorders), and many other diseases associated with the Fanconi syndrome. In Lowe syndrome, LMW proteinuria can be seen early in life even in the absence of clinically significant aminoaciduria or other renal tubular abnormalities [Laube et al 2004]. Thus, LMW may be the most sensitive early marker of the renal dysfunction occurring in this disorder.

Establishing the Diagnosis

Male proband. The diagnosis of Lowe syndrome is established in a male proband with typical clinical and laboratory findings and a hemizygous pathogenic variant in OCRL identified by molecular genetic testing (see Table 1).

Note: If a variant of unknown significance or no pathogenic variant is identified in a male with a clinical diagnosis consistent with Lowe syndrome, testing of inositol polyphosphate 5-phosphatase OCRL-1 activity in cultured skin fibroblasts is a possible option. Affected males have less than 10% normal activity of the enzyme. Such testing is abnormal in more than 99% of affected males and was shown to have high negative predictive value for Lowe syndrome in individuals referred with only partial overlap with Lowe syndrome phenotype who had no pathogenic variant found in OCRL [Hichri et al 2011].

Female proband. The diagnosis of Lowe syndrome in females is rare but can be established in a female proband with the same clinical and laboratory findings as a male proband and a heterozygous pathogenic variant in OCRL identified by molecular genetic testing. If a diagnosis of Lowe syndrome is established in a female, it is recommended that the clinician search for two pathogenic variants (one on each X chromosome) or an X-autosome translocation or other biologic cause for highly skewed inactivation of the X chromosome carrying the normal allele in a female heterozygote [Mueller et al 1991, Cau et al 2006].

Molecular Genetic Testing

Approaches can include a combination of gene-targeted testing (single-gene testing, multigene panel) and comprehensive genomic testing (chromosomal microarray analysis, exome sequencing, exome array, genome sequencing) depending on the phenotype.

Gene-targeted testing requires that the clinician determine which gene(s) are likely involved, whereas genomic testing does not. Because the phenotype of Lowe syndrome is broad, individuals with the distinctive findings described in Suggestive Findings are likely to be diagnosed using gene-targeted testing (see Option 1), whereas those with atypical features or in whom the diagnosis of Lowe syndrome has not been considered are more likely to be diagnosed using genomic testing (see Option 2).

Option 1. When the phenotypic and laboratory findings suggest the diagnosis of Lowe syndrome, molecular genetic testing approaches can include single-gene testing or use of a multigene panel:

  • Single-gene testing. Sequence analysis of OCRL detects small intragenic deletions/insertions and missense, nonsense, and splice site variants. If no pathogenic variant is found, perform gene-targeted deletion/duplication analysis to detect intragenic deletions or duplications.
  • A multigene panel that includes OCRL and other genes of interest (see Differential Diagnosis) is most likely to identify the genetic cause of the condition while limiting identification of variants of uncertain significance and pathogenic variants in genes that do not explain the underlying phenotype. Note: (1) The genes included in the panel and the diagnostic sensitivity of the testing used for each gene vary by laboratory and are likely to change over time. (2) Some multigene panels may include genes not associated with the condition discussed in this GeneReview. (3) In some laboratories, panel options may include a custom laboratory-designed panel and/or custom phenotype-focused exome analysis that includes genes specified by the clinician. (4) Methods used in a panel may include sequence analysis, deletion/duplication analysis, and/or other non-sequencing-based tests.
    For this disorder a multigene panel that also includes deletion/duplication analysis is recommended (see Table 1).
    For an introduction to multigene panels click here. More detailed information for clinicians ordering genetic tests can be found here.

Option 2. When the diagnosis of Lowe syndrome is not considered because an individual has atypical phenotypic features, comprehensive genomic testing (which does not require the clinician to determine which gene[s] are likely involved) is the best option. Exome sequencing is the most commonly used genomic testing method; genome sequencing is also possible.

If exome sequencing is not diagnostic, exome array (when clinically available) may be considered to detect (multi)exon deletions or duplications that cannot be detected by sequence analysis.

For an introduction to comprehensive genomic testing click here. More detailed information for clinicians ordering genomic testing can be found here.

Table 1.

Molecular Genetic Testing Used in Lowe Syndrome

Gene 1MethodProportion of Probands with a Pathogenic Variant 2 Detectable by Method
OCRL Sequence analysis 3~95% 4
Gene-targeted deletion/duplication analysis 5~5% 4
KaryotypeRare 6
1.

See Table A. Genes and Databases for chromosome locus and protein.

2.

See Molecular Genetics for information on allelic variants detected in this gene.

3.

Sequence analysis detects variants that are benign, likely benign, of uncertain significance, likely pathogenic, or pathogenic. Variants may include small intragenic deletions/insertions and missense, nonsense, and splice site variants; typically, exon or whole-gene deletions/duplications are not detected. For issues to consider in interpretation of sequence analysis results, click here.

4.
5.

Gene-targeted deletion/duplication analysis detects intragenic deletions or duplications. Methods used may include a range of techniques such as quantitative PCR, long-range PCR, multiplex ligation-dependent probe amplification (MLPA), and a gene-targeted microarray designed to detect single-exon deletions or duplications.

6.

Translocations between an autosome and an X chromosome with a breakpoint through OCRL (Xq26.1) have been observed in females with Lowe syndrome [Hodgson et al 1986, Reilly et al 1988, Mueller et al 1991]; therefore, in an individual with Lowe syndrome in whom a pathogenic variant has not been detected by other methods, karyotype may be considered.

Clinical Characteristics

Clinical Description

Usually only males have the disorder. A few affected females with the clinical manifestations of Lowe syndrome have been reported [Cau et al 2006].

The major clinical manifestations found in males with Lowe syndrome involve the eyes, central nervous system, and kidneys. Nearly all post-pubertal heterozygous females have lens opacities; a few will have additional findings. With the wide availability of molecular genetic testing, phenotypic heterogeneity appears to be substantially greater than previously suspected, such that individuals who lack certain features of Lowe syndrome can still have pathogenic variants in OCRL.

Males

Eyes. Dense congenital cataracts, formed as a result of abnormal metabolism or migration of the embryonic lens epithelium, are found in all affected boys. Although present at birth, the cataracts may not be detected until a few weeks of life. Rarely, the lens opacities are so mild that they do not affect visual development, even into the teen years.

  • Microphthalmos and enophthalmos, related to the lens abnormality, are noted occasionally.
  • Infantile glaucoma, present in approximately 50% of affected males, is difficult to control and often results in buphthalmos (enlarged eyes) and progressive visual loss [McSpadden 2000, Nussbaum & Suchy 2001]. Often the glaucoma is not detected until after the lenses have been removed. The glaucoma is severe and requires surgical, rather than medical, management.
  • Strabismus, retinal dystrophy, secondary corneal scarring, and calcific band keratopathy with keloid formation [Cibis et al 1982] may cause additional visual impairment [McSpadden 2000, Nussbaum & Suchy 2001].

All boys have impaired vision; corrected acuity is rarely better than 20/100 [McSpadden 2000, Nussbaum & Suchy 2001]. With decreased visual acuity, nystagmus develops early in life, even with early and uncomplicated surgery. Self-stimulatory activity also increases, i.e., rhythmic flapping of the hands, eye rubbing, and repetitive rocking movements. Despite aggressive intervention, visual disability may progress to blindness.

Central nervous system. Generalized infantile hypotonia is noted soon after birth and is of central origin. Deep tendon reflexes are usually absent. Hypotonia may slowly improve with age, but neither normal motor tone nor strength is ever achieved.

  • Feeding difficulties in infancy associated with poor head control, sucking, or swallowing may be a consequence of the hypotonia.
  • Decreased motor tone also results in delayed motor milestones. Independent ambulation occurs in approximately 25% of boys between age three and six years and in 75% by age six to 13 years. Some never walk, requiring the use of a wheelchair for mobility [McSpadden 2000].

Approximately 50% of affected boys have seizure disorders, most often of the generalized type and usually starting before age six years [McSpadden 2000].

Behavior problems (i.e., self-stimulation or stereotypic and obsessive-compulsive behaviors) are frequent and include many problems common to visually and intellectually handicapped individuals. Occasionally, violent tantrums or aggressive and self-abusive behaviors occur [Charnas & Gahl 1991, Kenworthy et al 1993].

Almost all affected males have some degree of intellectual impairment. Between 10% and 25% of affected males function in the low-normal or borderline range, approximately 25% function in the mild-to-moderate range, and 50%-65% function in the severe-to-profound range of intellectual disability [Kenworthy et al 1993]. Delayed language development is evident in early childhood. Most individuals learn to communicate verbally to some extent by age seven years; some eventually become quite verbal [McSpadden 2000]. Love of music and rhythm are notable.

As adults, most affected men reside with their families. A few are functional enough to live in a group home or even independently with appropriate assistance and guidance.

Kidneys. Affected boys have varying degrees of proximal renal tubular dysfunction of the renal Fanconi type. The features of symptomatic Fanconi syndrome do not usually become manifest until after the first few months of life, except for low molecular-weight (LMW) proteinuria.

  • LMW proteins are normally filtered by the glomerulus, then reabsorbed in the proximal tubule through endocytosis and metabolized in lysosomes in proximal tubular cells.
  • When reabsorption and/or metabolism are dysfunctional, LMW proteins, including retinol-binding protein, beta-2-microglobulin, and the lysosmal enzyme N-acetyl glucosaminidase, are lost in the urine. LMW proteinuria has been identified as early as just after birth [Laube et al 2004] and may be the most sensitive early marker for renal involvement of Lowe syndrome.

The molecular size of albumin is at the upper end of the size range for LMW proteins, so the small percentage of albumin that is normally filtered by the glomerulus is also reabsorbed and metabolized by the proximal tubule via the LMW protein transport process.

In Lowe syndrome, proximal renal tubular dysfunction often leads to clinically apparent albuminuria (urine dipstick albumin 1-4+; nephrotic range proteinuria >1 g/m2/day in more than half), while serum albumin remains normal [Bökenkamp & Ludwig 2016]. Albuminuria is better known as a marker of glomerular injury in other diseases such as diabetes mellitus; in Lowe syndrome it likely reflects proximal tubular dysfunction, especially early in life before chronic renal failure occurs.

All boys have LMW proteinuria and albuminuria, likely due to downstream disordered endocytosis and postendocytic membrane trafficking in the proximal tubular cell [Cui et al 2010, De Matteis et al 2017]. Most boys have aminoaciduria [Bökenkamp & Ludwig 2016]. Some boys develop full-blown renal Fanconi syndrome with bicarbonaturia and renal tubular acidosis, phosphaturia with hypophosphatemia and renal rickets, sodium and potassium wasting, and polyuria with an apparent urine-concentrating defect from the massive solute loss in the urine. Few of these boys have renal glucose wasting, which is frequently observed in other diseases with full-spectrum renal Fanconi syndrome [Bockenhauer et al 2008, Bökenkamp & Ludwig 2016, Zaniew et al 2018]. Other boys have little or no bicarbonaturia and phosphaturia, but LMW proteinuria and hypercalciuria with nephrocalcinosis and nephrolithiasis (calcium oxalate and calcium phosphate stones) similar to Dent disease [Bockenhauer et al 2008, Bökenkamp & Ludwig 2016].

Progressive glomerulosclerosis likely results from progressive renal tubular injury, which eventually may lead to chronic kidney disease (CKD) and end-stage renal disease (ESRD) between the second and fourth decades of life [McSpadden 2000, Nussbaum & Suchy 2001, Zaniew et al 2018].

Life span. Most males do not live past age 40 years. In older individuals, death has been related to progressive renal failure or scoliosis. Death from dehydration, pneumonia, and infections occurs at all ages [McSpadden 2000].

Short stature. Although birth length is usually normal, linear growth velocity is below normal and short stature becomes evident by age one year. The average adult height is approximately 155 cm [McSpadden 2000]. CKD and acidosis along with renal rickets or other bone disease may contribute to the short stature. Some boys have been treated with growth hormone, resulting in an increase in height but persistence of short stature for age [Zaniew et al 2018].

Feeding and gastrointestinal concerns

  • Slow weight gain may occur because of insufficient caloric intake.
  • Gastroesophageal reflux, most common in infancy, may be seen at any age.
  • Aspiration of food along with a decreased ability to cough effectively to clear lung fields may lead to atelectasis, pneumonia, or chronic lung disease.
  • Poor abdominal muscle tone increases the risk for chronic constipation and the development of (predominantly inguinal) hernias.

Bone disease in affected boys may be related to Fanconi syndrome with phosphaturia, inadequate renal production of 1,25-dihydroxyvitamin D, and chronic acidosis as well as CKD. The bone disease may appear as classic changes of rickets on bone radiographs.

However, even in the presence of well-corrected Fanconi syndrome and no findings of rickets, some boys have repeat pathologic bone fractures with poor healing and bone demineralization on radiographs or bone densitometry [E Brewer, personal observation].

Whether some of the bone disease is related to inactivity resulting from muscle hypotonia and immobilization in severely affected boys or to a primary defect in bone mineralization/molecular transport requires further study.

Other musculoskeletal concerns

  • Decreased truncal motor tone increases the risk of developing scoliosis, present in approximately 50% of affected boys [McSpadden 2000].
  • Hypermobile joints may result in joint dislocation, especially of the hips and knees.
  • In affected teenagers and adults, joint swelling, arthritis, tenosynovitis, and subcutaneous benign fibromas, often on the hands and feet and most especially in areas of repeated trauma, are noted frequently [Athreya et al 1983, Elliman & Woodley 1983].
  • Elevated serum creatine kinase (CK), AST, and LDH are typical in Lowe syndrome and likely due to abnormal muscle metabolism [Charnas et al 1991, Bökenkamp & Ludwig 2016]. Decreased plasma carnitine concentration has been reported in approximately one third of individuals with Lowe syndrome [Charnas et al 1991], but the need for or efficacy of carnitine supplementation has never been studied, and therapy continues to be individualized.

Genitourinary issues

  • Undescended testes (cryptorchidism) are noted in approximately one third of affected boys [McSpadden 2000, Recker et al 2015]. Isolated LH elevation at baseline and on GnRH stimulation testing was observed in an infant with undescended testes [Warner et al 2017].
  • Puberty may be delayed in onset; otherwise, male secondary sexual development is normal.

Teeth and skin findings. Dental malformations and generalized mobility of primary teeth with decreased or dysplastic dentin formation may also be related to a primary dental abnormality in Lowe syndrome [Harrison et al 1999].

Superficial cysts may occur in the mouth and on the skin, especially the scalp, lower back and buttocks.The skin cysts may become painful and occasionally infected. Histologic examination revealed epidermal cysts in which the dermis was lined by several layers of stratified squamous epithelium with a granular layer and filled with keratin flakes [Ikehara & Utani 2017]. Cysts have also been found in imaging studies of the kidneys and brain. These findings suggest that an abnormality in connective tissue may also be involved in the pathogenesis of the disorder [McSpadden 2000, Kim et al 2014, Murakami et al 2018].

Coagulation disorder. The OCRL-1 protein is found in human platelets. Prolonged or delayed bleeding following surgery, such as cataract extraction has been reported. An intrinsic platelet defect in these individuals that can be detected using a platelet function analyzer (PFA-100) was identified; other coagulation profile related tests, including platelet counts, gave normal results [Lasne et al 2010]. In another study, thrombocytopenia/low normal platelets were found in about 20% [Recker et al 2015].

Females

Approximately 95% of postpubertal heterozygous females have characteristic findings in the lens of each eye on slit lamp examination through a dilated pupil by an experienced ophthalmologist. The lens findings have correlated with the results of molecular genetic studies in predicting heterozygosity for the pathogenic variant in OCRL in postpubertal females [Lin et al 1999, McSpadden 2000, Röschinger et al 2000, Nussbaum & Suchy 2001]. While the lens findings may appear in prepubertal females as well (especially the less common axial posterior central opacity), their absence does not exclude the possibility of heterozygosity.

Most heterozygous females show numerous irregular, punctate, smooth, off-white (white to gray) opacities, present in the lens cortex, more in the anterior cortex than the posterior cortex, and distributed in radial bands that wrap around the lens equator. Classically, the nucleus is spared. On retroillumination, the opacities are distributed in a radial, spoke-like pattern and can be relatively dense in a wedge shape comparable to an hour or two on the face of a clock, alternating with a similar-sized wedge with few to no opacities.

A few heterozygous females (~10%) have a dense central precapsular dead-white cataract at the posterior pole of the lens that may be visually significant if it is large. Similarly, the cataracts in some heterozygous females may become visually significant by the fourth decade and require surgery without the diagnostic importance being recognized.

The manifestations of Lowe syndrome besides those seen in the lens are not observed in heterozygous females unless there is either rare X;autosome translocation with the X chromosome breakpoint at OCRL or extremely skewed X inactivation. In an example of the latter, a female with two structurally normal X chromosomes showed classic, severe Lowe syndrome as a result of a familial defect in X inactivation inherited from her father. The paternally derived X chromosome containing a normal OCRL gene remained inactive in 100% of cells, while the maternally derived X chromosome carrying a pathogenic variant of ORCL was active in 100% of cells tested [Cau et al 2006].

Genotype-Phenotype Correlations

To date, correlation of genotype with phenotype has not been established. Differing clinical courses have been noted in unrelated individuals with the same OCRL pathogenic variant [Leahey et al 1993]. It is also now apparent that pathogenic variants in OCRL that result in total loss of OCRL expression occur both in individuals with Lowe syndrome and in individuals with the allelic disorder, Dent disease, but there have not been families in which one affected male has Lowe syndrome and a male relative with the same pathogenic variant has Dent disease.

Penetrance

Penetrance is complete, with variability in severity of phenotype in affected males within any given family.

Nomenclature

Oculocerebrorenal syndrome, the formal term for this disorder, is synonymous with Lowe syndrome, and may be preferred to avoid eponymous syndrome nomenclature.

Prevalence

Lowe syndrome is an uncommon, pan ethnic disorder with an estimated prevalence of 1:500,000 in the general population, based on observations of the American Lowe Syndrome Association and the Italian Association of Lowe syndrome [Bökenkamp & Ludwig 2016].

The disorder has been seen in America, Europe, Australia, Japan, and India and is believed to occur worldwide.

Differential Diagnosis

Low molecular-weight (LMW) proteinuria is a feature of Fanconi syndrome and can also be seen in other conditions including cystinosis, nephrotoxic drug injury to the tubules (e.g., aminoglycosides), and acute tubulointerstitial renal transplant rejection with tubular injury. However, the LMW proteinuria appears to be a more prominent feature of renal tubular dysfunction in Lowe syndrome and Dent disease than in these other disorders.

Like Lowe syndrome, generalized congenital infections (e.g., rubella) are associated with a combination of congenital or neonatal-onset cataracts, hypotonia, proximal renal tubular dysfunction, and/or delayed development and should be considered in the differential diagnosis of Lowe syndrome. Genetic disorders that may be associated with these features are summarized in Table 2.

Table 2.

Disorders to Consider in the Differential Diagnosis of Lowe Syndrome

DiffDx DisorderGene(s)MOIClinical Features of DiffDx Disorder
Overlapping w/Lowe syndromeDistinguishing from Lowe syndrome
Zellweger spectrum disorder PEX1
PEX6
PEX12
PEX26
PEX10
PEX2
PEX5
PEX13
PEX16
PEX3
PEX19
PEX14
PEX11β 		AR
  • Hypotonia
  • May have congenital cataracts
  • Retinal dystrophy
  • Renal cysts
  • DD
  • Poor feeding
  • Neonatal seizures common
  • Distinctive craniofacial features (e.g., flat face, broad nasal bridge, large anterior fontanelle, widely split sutures)
  • SNHL
  • Liver dysfunction
  • Bony stippling (chondrodysplasia punctata) of patella(e) & other long bones may occur.
Nance-Horan syndrome
(OMIM 302350)		 NHS XL
  • Congenital cataracts
  • Hypotonia
  • ID
  • Dental anomalies (e.g., cone-shaped incisors & supernumerary teeth)
  • Heterozygous females have Y-shaped sutural cataracts & may have dental anomalies.
  • Microcornea
  • No renal abnormalities
  • Facial dysmorphisms (e.g., anteverted pinnae)
  • Absence of characteristic facial appearance seen in Lowe syndrome (i.e., sunken orbits & bitemporal hollowing)
Smith-Lemli-Opitz syndrome DHCR7 AR
  • Congenital cataracts
  • Hypotonia
  • Renal anomalies (most commonly renal hypoplasia or agenesis, renal cortical cysts, hydronephrosis, & structural anomalies of collecting system)
  • Moderate-to-severe ID
  • Prenatal & postnatal growth restriction
Multiple major & minor malformations incl:
  • Microcephaly
  • Distinctive facial features
  • Cleft palate
  • Cardiac defects
  • Underdeveloped external genitalia in males
  • Postaxial polydactyly
  • 2-3 toe syndactyly
Congenital myotonic dystrophy type 1 DMPK AD
  • Cataracts
  • ID
  • Infantile hypotonia; severe generalized weakness at birth
  • Respiratory insufficiency at birth
  • No significant renal disease
Disorders of mitochondrial oxidative phosphorylation 3See footnote 1.
  • Seizures
  • Hypotonia at birth or developing in early infancy
  • Renal findings incl Fanconi syndrome, RTA, & renal failure are frequent (esp in Kearns-Sayre syndrome, mt encephalomyopathy & mt depletion syndrome) 3
  • Common features of mt disease incl: ptosis, external ophthalmoplegia, proximal myopathy, exercise intolerance, cardiomyopathy, sensorineural deafness, optic atrophy, pigmentary retinopathy, diabetes mellitus
  • CNS findings (often fluctuating): encephalopathy, dementia, migraine, stroke-like episodes, ataxia
  • Note: Congenital cataract is seen in GFER-related mt myopathy (OMIM 613076) but is NOT typical for mt disorders
Cystinosis CTNS AR
  • Renal Fanconi syndrome 2; CKD
  • Poor growth; in untreated persons, failure to grow is generally noticed at age 6-9 mos.
  • Retinal disease
  • Typical cystine crystals on slit lamp exam of cornea
  • No cataracts
  • Intellectual abilities low-normal
  • No hypotonia
Donnai-Barrow syndrome LRP2 AR
  • LMW proteinuria, hypercalciuria, nephrocalcinosis, nephrolithiasis, CKD 4
  • Cataract may be seen in juveniles w/Donnai-Barrow syndrome.
  • High myopia
  • No congenital cataracts
  • SNHL
  • Hypertelorism
  • Large anterior fontanelles
  • Hypotonia not typical; motor milestones only slightly delayed

AD = autosomal dominant; AR = autosomal recessive; CKD = chronic kidney disease; CNS = central nervous system; DD = developmental delay; DiffDx = differential diagnosis; ID = intellectual disability; LMW = low molecular-weight; MOI = mode of inheritance; mt = mitochondrial; RTA = renal tubular acidosis; SNHL = sensorineural hearing loss; XL = X-linked

1.

Mitochondrial disorders may be caused by defects of nuclear DNA or mtDNA: nuclear gene defects may be inherited in an autosomal recessive, autosomal dominant, or X-linked manner, mitochondrial DNA defects are transmitted by maternal inheritance.

2.

Cystine-depleting therapy begun just after birth can attenuate the Fanconi syndrome.

3.
4.

Management

Evaluations Following Initial Diagnosis

To establish the extent of disease in an individual diagnosed with Lowe syndrome, the evaluations summarized in Table 3 (if not performed as part of the evaluation that led to the diagnosis) are recommended.

Table 3.

Recommended Evaluations Following Initial Diagnosis in Individuals with Lowe Syndrome

System/
Concern		EvaluationComment
Eyes Ophthalmologic exam to assess for cataract & glaucomaBehavior problems may necessitate use of anesthesia for exam.
CNS
  • Developmental & behavior assessments
  • EEG if seizures present to optimize therapy
Kidneys Assess renal tubular function.Tests should incl:
  • Serum electrolytes, glucose, calcium, phosphorus, creatinine
  • Simultaneous urinalysis, urine pH, sodium, potassium, chloride, calcium, phosphorus, creatinine, amino acids, protein & retinol-binding protein, &/or N-acetyl glucosaminidase (if available) 1
If hematuria or hypercalciuria is present, renal ultrasound to look for nephrolithiasis or nephrocalcinosis.
If aciduria or phosphaturia present, test serum 1,25-dihydroxy vitamin D & parathyroid hormone plus bone radiographs to evaluate for renal rickets.
Growth/
Feeding
  • Growth parameters
  • Infants assessed for feeding problems & gastroesophageal reflux, incl a pH probe study
Skeletal Radiographs for bone pain or point tenderness to evaluate for fractures
Dental Thorough clinical exam after tooth eruptionGeneralized mobility of all primary teeth as well as subrachitic changes due to renal rickets
Hematologic Alert providers performing any surgical interventions of risk for delayed bleeding after apparent hemostasis in immediate post-op period.
Other Consultation w/clinical geneticist &/or genetic counselor
1.

Interpretation of these results allows diagnosis of type 2 renal tubular acidosis, hypokalemia, phosphate wasting with decreased tubular reabsorption of phosphate (TRP), hypercalciuria (urine calcium/creatinine ratio >0.02), amino aciduria, albuminuria (urine dipstick-positive albumin and urine protein/creatinine ratio >0.2), LMW proteinuria, and CKD (serum creatinine).

Treatment of Manifestations

Management of the varying clinical problems usually requires more than one medical specialist; experts in pediatric ophthalmology, nephrology, clinical biochemical genetics, metabolism, nutrition, endocrinology, neurology, child development, behavior, rehabilitation, general surgery, orthopedics, or dentistry may be involved.

Table 4.

Treatment of Manifestations in Individuals with Lowe Syndrome

Manifestation/
Concern		TreatmentConsiderations/Other
Cataract
  • Early removal to promote proper visual stimulation & development
  • Postoperative glasses to improve vision & replace the crystalline lens power
NOT recommended:
  • Surgical implantation of artificial lenses (due to high prevalence of infantile glaucoma)
  • Contact lenses (due to risk for corneal keloids)
Glaucoma Manage w/standard medical & surgical measures.Often difficult to control medically & almost invariably requires surgery
Developmental
delays 		Early infant therapy, preschool intervention program & IEP throughout schooling
Behavior
problems 		Behavior modification programMedication may also be needed for behavior control.
Seizures Anticonvulsant medication
Renal tubular dysfunction Oral supplements of sodium & potassium bicarbonate or citrate to correct acidosis & hypokalemiaDoses need to be titrated to individual needs based on "trough" blood concentrations of serum electrolytes (sodium, potassium, chloride, & total carbon dioxide).
Treatment w/oral phosphate, along w/oral calcitriol (1,25-dihydroxyvitamin D3) to correct hypophosphatemia & renal rickets from renal tubular dysfunctionDoses should also be titrated to individual needs based on trough blood concentration for phosphorus & serum concentrations of 1,25-dihydroxyvitamin D, calcium, & intact parathyroid hormone.
IV replacement of fluids, bicarbonate, & electrolytes at times of illness assoc w/vomiting & diarrhea or when fasting (e.g., w/surgical procedures)
ESRD Chronic dialysis & renal transplant may be successful in some persons.Progressive renal tubular injury → progressive glomerulosclerosis & CKD → ESRD (over yrs, usually by 2nd-4th decade)
Growth/
Feeding 		Growth hormone therapy → improved growth velocity in some boys.Potential benefits of such therapy must be weighed against its costs/limitations.
  • NG tube feedings or feeding gastrostomy w/or w/o fundoplication may be necessary to treat infant feeding & nutrition problems related to hypotonia.
  • Standard treatment for gastroesophageal reflux, if present
Scoliosis
& joint
hypermobility 		Bracing or surgery may be performed to arrest or correct severe or progressive scoliosis & joint hypermobility.
Fibromas &
cutaneous cysts 		Resection may be needed if painful, recurrently infected, or limiting function.

CKD = chronic kidney disease; ESRD = end-stage renal disease; IEP = individualized education program; NG = nasogastric

Surveillance

Table 5.

Recommended Surveillance for Individuals with Lowe Syndrome

System/
Concern		EvaluationFrequency
Eyes Intraocular pressure monitoringEvery 6 mos life long
Other ophthalmic eval
  • As determined by specialist based on type & severity of eye abnormality
  • Promptly w/any signs of ↑ intraocular pressure (e.g., excessive tearing, eye rubbing, change in clarity/transparency of cornea)
CNS Developmental progress assessed & educational plan updated2x/yr for 1st 3 yrs, then annually
Brain imaging for any regression in abilities
Kidneys Kidney function assessment 1At least annually
  • If on supplemental bicarbonate or citrate, phosphorus or calcitriol or other vitamin D analog, need kidney function assessment 1 w/blood & urine tests
  • May need serum vitamin D-25 hydroxy to assess for parent vitamin D deficiency
Every 3-6 mos; more often after dose changes
Radiographs of long bones & growth plates if renal bone disease is presentRegular intervals as needed, but no more than every 6 mos
Growth Height/length & weight
  • Every 1-2 mos in infants
  • Every 3-6 mos in older children & adolescents
  • Every 3 mos if on growth hormone
Skeletal Monitor scoliosis & joint hypermobilityAnnually
Dental Exams by pediatric dentist2x/yr
1.

Testing includes measurement of (a) serum concentrations of electrolyte, blood urea nitrogen (BUN), creatinine, calcium, phosphorus, albumin, intact parathyroid hormone, and 1,25-dihydroxyvitamin D and (b) urinalysis and random urine protein, calcium, and creatinine.

Agents/Circumstances to Avoid

Corneal contact lenses. Because of the associated risks of corneal keloid formation and the inherent difficulties that the person with Lowe syndrome has in managing personal contact lens care, conventional eye glasses seem safer than corneal contact lenses.

Artificial lens implants. Although some infants have had primary intraocular lens implantation at the time of cataract surgery, the associated risk of glaucoma appears higher in those infants with artificial lens implants. Therefore, artificial lens implants should be used with extreme caution, with intraocular pressure carefully monitored (under anesthesia if required) on a continual basis.

Evaluation of Relatives at Risk

See Genetic Counseling for issues related to testing of at-risk relatives for genetic counseling purposes.

Therapies Under Investigation

Search ClinicalTrials.gov in the US and EU Clinical Trials Register in Europe for access to information on clinical studies for a wide range of diseases and conditions. Note: There may not be clinical trials for this disorder.

Genetic Counseling

Genetic counseling is the process of providing individuals and families with information on the nature, mode(s) of inheritance, and implications of genetic disorders to help them make informed medical and personal decisions. The following section deals with genetic risk assessment and the use of family history and genetic testing to clarify genetic status for family members; it is not meant to address all personal, cultural, or ethical issues that may arise or to substitute for consultation with a genetics professional. —ED.

Mode of Inheritance

Lowe syndrome is inherited in an X-linked manner.

Risk to Family Members

Parents of a male proband

  • The father of an affected male will not have the disorder, nor will he be hemizygous for the ORCL pathogenic variant; therefore, he does not require further evaluation/testing.
  • In a family with more than one affected individual, the mother of an affected male is an obligate heterozygote.
    Note: If a woman has more than one affected child and no other affected relatives and if the OCRL pathogenic variant cannot be detected in her leukocyte DNA, she most likely has germline mosaicism. In one study group, two (4.5%) of 44 women were found to have germline mosaicism [Satre et al 1999, Monnier et al 2000].
  • If a male is the only affected family member, the mother may be a heterozygote or have germline mosaicism, or the affected male may have a de novo OCRL pathogenic variant, in which case the mother is not a heterozygote. De novo pathogenic variants have been reported in approximately 32% of males with Lowe syndrome [Satre et al 1999, Monnier et al 2000].
  • The mother of a child with Lowe syndrome who represents a simplex case (i.e., a single occurrence in a family) should be thoroughly evaluated by an experienced ophthalmologist for the characteristic punctate anterior radial lens opacities seen in female heterozygotes.

Sibs of a male proband. The risk to sibs of a proband depends on the genetic status of the mother:

  • If the mother of the proband is heterozygous for an OCRL pathogenic variant, the chance of transmitting it in each pregnancy is 50%. Males who inherit the pathogenic variant will be affected; females who inherit the variant will be heterozygotes and will usually develop characteristic findings in the lens of each eye (see Clinical Description, Females).
  • If the proband represents a simplex case (i.e., a single occurrence in a family) and if the OCRL pathogenic variant cannot be detected in the leukocyte DNA of the mother, the recurrence risk to sibs is still increased due to the possibility of maternal germline mosaicism which has been reported in five families with Lowe syndrome [Bökenkamp & Ludwig 2016].

Offspring of a male proband. Affected males are not known to reproduce.

Other family members. The proband's maternal aunts may be at risk of being heterozygous and the aunt's offspring, depending on their sex, may be at risk of being heterozygous or of being affected.

Note: Molecular genetic testing may be able to identify the family member in whom a de novo pathogenic variant arose, information that could help determine genetic risk status of the extended family.

Heterozygote Detection

Molecular genetic testing of at-risk female relatives to determine their genetic status is most informative if the OCRL pathogenic variant has been identified in the proband.

Slit lamp examination. Approximately 95% of heterozygous females older than age 15 years are observed to have characteristic findings in the lens of the eye on slit lamp examination by an experienced ophthalmologist using both direct and retroillumination; thus, ophthalmologic exam may be used as a method of heterozygote detection.

Biochemical enzymatic assays for inositol polyphosphate 5-phosphatase OCRL-1 activity are not accurate for heterozygote detection because of lyonization (random X-chromosome inactivation) in females [Lin et al 1999].

Related Genetic Counseling Issues

Family planning

  • The optimal time for determination of genetic risk, clarification of heterozygote status, and discussion of the availability of prenatal/preimplantation genetic testing is before pregnancy.
  • It is appropriate to offer genetic counseling (including discussion of potential risks to offspring and reproductive options) to young adult females who are heterozygotes, or are at risk of being heterozygotes.

Prenatal Testing and Preimplantation Genetic Testing

Once the OCRL pathogenic variant has been identified in an affected family member, prenatal and preimplantation genetic testing are possible.

Because of the relatively high rate (4.5%) of germline mosaicism, every mother of a male with Lowe syndrome, even with a negative family history, should be offered prenatal DNA testing if the pathogenic variant in her son is known, even if the results of dilated slit lamp examination or DNA testing suggest that she is not a heterozygote [McSpadden 2000].

Differences in perspective may exist among medical professionals and within families regarding the use of prenatal testing. While most centers would consider use of prenatal testing to be a personal decision, discussion of these issues may be helpful.

Resources

GeneReviews staff has selected the following disease-specific and/or umbrella support organizations and/or registries for the benefit of individuals with this disorder and their families. GeneReviews is not responsible for the information provided by other organizations. For information on selection criteria, click here.

Molecular Genetics

Information in the Molecular Genetics and OMIM tables may differ from that elsewhere in the GeneReview: tables may contain more recent information. —ED.

Table A.

Lowe Syndrome: Genes and Databases

GeneChromosome LocusProteinLocus-Specific DatabasesHGMDClinVar
OCRL Xq26​.1 Inositol polyphosphate 5-phosphatase OCRL OCRL @ LOVD at NCBI OCRL OCRL

Data are compiled from the following standard references: gene from HGNC; chromosome locus from OMIM; protein from UniProt. For a description of databases (Locus Specific, HGMD, ClinVar) to which links are provided, click here.

Table B.

OMIM Entries for Lowe Syndrome (View All in OMIM)

300535OCRL INOSITOL POLYPHOSPHATE-5-PHOSPHATASE; OCRL
309000LOWE OCULOCEREBRORENAL SYNDROME; OCRL

Molecular Pathogenesis

Lowe syndrome results from loss of inositol polyphosphate 5-phosphatase OCRL-1 (phosphatidylinositol polyphosphate 5-phosphatase OCRL-1) activity. Although the exact mechanisms are unclear, the absence of the protein and elevated PtdIns (4,5) P2 levels may affect these processes, which may influence all – or a combination of some – of the following:

  • Cell membrane composition
  • Actin cytoskeletal organization
  • Endocytosis
  • Lysosomal-autophagic pathway
  • Primary ciliary synthesis and function

Loss of OCRL-1 ultimately leads to abnormal differentiation, cell migration, and function in certain cell types (i.e., renal tubule or lens epithelium). Such changes could result in the birth defects and other clinical manifestations of Lowe syndrome [Zhang et al 1995, Suchy & Nussbaum 2002, Ungewickell et al 2004, De Matteis et al 2017].

The enzyme is present in the trans-Golgi network and the endosomal and lysosomal compartment of a variety of cell types, including brain, skeletal muscle, heart, kidney (cultured proximal renal tubular cells), lung, ovary, testis, cultured fibroblasts, placenta, chorionic villi samples, and cultured amniocytes.

Mechanism of disease causation. Lowe syndrome occurs through a loss-of-function mechanism. Reduced activity or absence of inositol polyphosphate 5-phosphatase OCRL-1 leads to elevated intracellular levels of its substrate, phosphatidylinositol (4,5) bisphosphate [PtdIns (4,5) P2] [Zhang et al 1998], resulting in highly pleiotropic effects on a number of cellular processes. These processes include a defect in intracellular protein trafficking [Vicinanza et al 2011], impaired endocytic tubular transport [Festa et al 2019] and primary ciliary function [Luo et al 2013]. Impaired endocytosis is most closely implicated in the low molecular-weight proteinuria and other tubular defects, while ciliary function abnormalities are more closely implicated in the ophthalmologic complications.

Of the identified pathogenic variants, 93% have been located in exons 10-18 and exons 19-23 of OCRL, particularly in exon 15 [Satre et al 1999, Monnier et al 2000, Nussbaum 2001, Nussbaum & Suchy 2001]. Recent data suggest an association between pathogenic variants in the first eight exons of OCRL and Dent disease [Shrimpton et al 2009, Hichri et al 2011]; however, the correlation is not perfect [Tosetto et al 2009].

References

Literature Cited

  • Anglani F, Terrin L, Brugnara M, Battista M, Cantaluppi V, Ceol M, Bertoldi L, Valle G, Joy MP, Pober BR, Longoni M. Hypercalciuria and nephrolithiasis: Expanding the renal phenotype of Donnai-Barrow syndrome. Clin Genet. 2018;94:187–8. [PMC free article: PMC5995642] [PubMed: 29532936]
  • Athreya BH, Schumacher HR, Getz HD, Norman ME, Borden S 4th, Witzleben CL. Arthropathy of Lowe's (oculocerebrorenal) syndrome. Arthritis Rheum. 1983;26:728–35. [PubMed: 6860374]
  • Bockenhauer D, Bökenkamp A, van't Hoff W, Levtchenko E, Kist-van Holthe JE, Tasic V, Ludwig M. Renal phenotype in Lowe Syndrome: a selective proximal tubular dysfunction. Clin J Am Soc Nephrol. 2008;3:1430–6. [PMC free article: PMC2518783] [PubMed: 18480301]
  • Bökenkamp A, Böckenhauer D, Cheong HI, Hoppe B, Tasic V, Unwin R, Ludwig M. Dent-2 disease: a mild variant of Lowe syndrome. J Pediatr. 2009;155:94–9. [PubMed: 19559295]
  • Bökenkamp A, Ludwig M. The oculocerebrorenal syndrome of Lowe: an update. Pediatr Nephrol. 2016;31:2201–12. [PMC free article: PMC5118406] [PubMed: 27011217]
  • Cau M, Addis M, Congiu R, Meloni C, Cao A, Santaniello S, Loi M, Emma F, Zuffardi O, Ciccone R, Sole G, Melis MA. A locus for familial skewed X chromosome inactivation maps to chromosome Xq25 in a family with a female manifesting Lowe syndrome. J Hum Genet. 2006;51:1030–6. [PubMed: 16955230]
  • Charnas LR, Gahl WA. The oculocerebrorenal syndrome of Lowe. Adv Pediatr. 1991;38:75–107. [PubMed: 1927708]
  • Charnas LR, Bernardini I, Rader D, Hoeg JM, Gahl WA. Clinical and laboratory findings in the oculocerebrorenal syndrome of Low, with special reference to growth and renal function. N Engl J Med. 1991;324:1318–25. [PubMed: 2017228]
  • Cibis GW, Tripathi RC, Tripathi BJ, Harris DJ. Corneal keloid in Lowe's syndrome. Arch Ophthalmol. 1982;100:1795–9. [PubMed: 7138348]
  • Cui S, Guerriero CJ, Szalinski CM, Kinlough CL, Hughey RP, Weisz OA. OCRL1 function in renal epithelial membrane traffic. Am J Physiol Renal Physiol. 2010;298:F335–45. [PMC free article: PMC2822509] [PubMed: 19940034]
  • De Matteis MA, Staiano L, Emma F, Devuyst O. The 5-phosphatase OCRL in Lowe syndrome and Dent disease 2. Nature Reviews Nephrology. 2017;13:455–70. [PubMed: 28669993]
  • Elliman D, Woodley A. Tenosynovitis in Lowe syndrome. J Pediatr. 1983;103:1011. [PubMed: 6644416]
  • Festa BP, Berquez M, Gassama A, Amrein I, Ismail HM, Samardzija M, Staiano L, Luciani A, Grimm C, Nussbaum RL, De Matteis MA, Dorchies OM, Scapozza L, Wolfer DP, Devuyst O. OCRL deficiency impairs endolysosomal function in a humanized mouse model for Lowe syndrome and dent disease. Hum Mol Genet. 2019;28:1931–46. [PMC free article: PMC6548226] [PubMed: 30590522]
  • Finsterer J, Scorza FA. Renal manifestations of primary mitochondrial disorders. Biomed Rep. 2017;6:487–94. [PMC free article: PMC5431253] [PubMed: 28515908]
  • Harrison M, Odell EW, Sheehy EC. Dental findings in Lowe syndrome. . Pediatr Dent. 1999;21:425–8. [PubMed: 10633515]
  • Hichri H, Rendu J, Monnier N, Coutton C, Dorseuil O, Poussou RV, Baujat G, Blanchard A, Nobili F, Ranchin B, Remesy M, Salomon R, Satre V, Lunardi J. From Lowe syndrome to Dent disease: correlations between mutations of the OCRL1 gene and clinical and biochemical phenotypes. Hum Mutat. 2011;32:379–88. [PubMed: 21031565]
  • Hodgson SV, Heckmatt JZ, Hughes E, Crolla JA, Dubowitz V, Bobrow M. A balanced de novo X/autosome translocation in a girl with manifestations of Lowe syndrome. Am J Med Genet. 1986;23:837–47. [PubMed: 3953680]
  • Hoopes RR Jr, Shrimpton AE, Knohl SJ, Hueber P, Hoppe B, Matyus J, Simckes A, Tasic V, Toenshoff B, Suchy SF, Nussbaum RL, Scheinman SJ. Dent Disease with mutations in OCRL1. Am J Hum Genet. 2005;76:260–7. [PMC free article: PMC1196371] [PubMed: 15627218]
  • Ikehara S, Utani A. Multiple protrusive epidermal cysts on the scalp of a Lowe syndrome patient. J Dermatol. 2017;44:105–7. [PubMed: 27178641]
  • Kenworthy L, Park T, Charnas LR. Cognitive and behavioral profile of the oculocerebrorenal syndrome of Lowe. Am J Med Genet. 1993;46:297–303. [PubMed: 8488875]
  • Kim HK, Kim JH, Kim YM, Kim G-H, Lee BH, Choi J-H. Lowe syndrome: a single center’s experience in Korea. Korean J Pediatr. 2014;57:140–8. [PMC free article: PMC4000760] [PubMed: 24778696]
  • Lasne D, Baujat G, Mirault T, Lunardi J, Grelac F, Egot M, Salomon R, Bachelot-Loza C. Bleeding disorders in Lowe syndrome patients: evidence for a link between OCRL mutations and primary haemostasis disorders. Br J Haematol. 2010;150:685–8. [PubMed: 20629659]
  • Laube GF, Russell-Eggitt IM, van't Hoff WG. Early proximal tubular dysfunction in Lowe's syndrome. Arch Dis Child. 2004;89:479–80. [PMC free article: PMC1719890] [PubMed: 15102646]
  • Leahey AM, Charnas LR, Nussbaum RL. Nonsense mutations in the OCRL-1 gene in patients with the oculocerebrorenal syndrome of Lowe. Hum Mol Genet. 1993;2:461–3. [PubMed: 8504307]
  • Lin T, Lewis RA, Nussbaum RL. Molecular confirmation of carriers for Lowe syndrome. Ophthalmology. 1999;106:119–22. [PubMed: 9917791]
  • Luo N, Kumar A, Conwell M, Weinreb RN, Anderson R, Sun Y. Compensatory Role of Inositol 5-Phosphatase INPP5B to OCRL in Primary Cilia Formation in Oculocerebrorenal Syndrome of Lowe. PLoS One. 2013;8:e66727. [PMC free article: PMC3689662] [PubMed: 23805271]
  • McSpadden K. Living with Lowe Syndrome: A Guide for Families, Friends and Professionals. 3 ed. Lowe Syndrome Association, Inc. 2000.
  • Monnier N, Satre V, Lerouge E, Berthoin F, Lunardi J. OCRL1 mutation analysis in French Lowe syndrome patients: implications for molecular diagnosis strategy and genetic counseling. Hum Mutat. 2000;16:157–65. [PubMed: 10923037]
  • Mueller OT, Hartsfield JK Jr, Gallardo LA, Essig YP, Miller KL, Papenhausen PR, Tedesco TA. Lowe oculocerebrorenal syndrome in a female with a balanced X;20 translocation: mapping of the X chromosome breakpoint. Am J Hum Genet. 1991;49:804–10. [PMC free article: PMC1683175] [PubMed: 1897526]
  • Murakami Y, Wataya-Kaneda M, Iwatani Y, Kubota T, Nakano H, Katayama I. Novel mutation of OCRL1 in Lowe syndrome with multiple epidermal cysts. J Dermatol. 2018;45:372–3. [PubMed: 28516463]
  • Nussbaum RL. Lowe Syndrome OCRL1 Mutation Database. Available online. 2001. Accessed 4-28-22.
  • Nussbaum RL, Suchy SF. The oculocerebrorenal syndrome of Lowe (Lowe syndrome). In: Scriver CR, Beaudet AL, Sly WS, Valle D, eds. The Metabolic and Molecular Bases of Inherited Disease. 8 ed. Chap 252. New York, NY: McGraw-Hill; 2001:6257-66.
  • Recker F, Zaniew M, Bockenhauer D, Miglietti N, Bökenkamp A, Moczulska A, Rogowska-Kalisz A, Laube G, Said-Conti V, Kasap-Demir B, Niemirska A, Litwin M, Siten G, Chrzanowska KH, Krajewska-Walasek A, Szczepanska M, Pawlaczyk K, Sikora P, Ludwig M. Characterization of 28 novel patients expands the mutational and phenotypic spectrum of Lowe syndrome. Pediatr Nephrol. 2015;30:931–43. [PubMed: 25480730]
  • Reilly DS, Lewis RA, Ledbetter DH, Nussbaum RL. Tightly linked flanking markers for the Lowe oculocerebrorenal syndrome, with application to carrier assessment. Am J Hum Genet. 1988;42:748–55. [PMC free article: PMC1715172] [PubMed: 2895982]
  • Röschinger W, Muntau AC, Rudolph G, Roscher AA, Kammerer S. Carrier assessment in families with lowe oculocerebrorenal syndrome: novel mutations in the OCRL1 gene and correlation of direct DNA diagnosis with ocular examination. Mol Genet Metab. 2000;69:213–22. [PubMed: 10767176]
  • Satre V, Monnier N, Berthoin F, Ayuso C, Joannard A, Jouk PS, Lopez-Pajares I, Megabarne A, Philippe HJ, Plauchu H, Torres ML, Lunardi J. Characterization of a germline mosaicism in families with Lowe syndrome, and identification of seven novel mutations in the OCRL1 gene. Am J Hum Genet. 1999;65:68–76. [PMC free article: PMC1378076] [PubMed: 10364518]
  • Shrimpton AE, Hoopes RR Jr, Knohl SJ, Hueber P, Reed AA, Christie PT, Igarashi T, Lee P, Lehman A, White C, Milford DV, Sanchez MR, Unwin R, Wrong OM, Thakker RV, Scheinman SJ. OCRL1 mutations in Dent 2 patients suggest a mechanism for phenotypic variability. Nephron Physiol. 2009;112:27–36. [PubMed: 19390221]
  • Suchy SF, Nussbaum RL. The deficiency of PIP2 5-phosphatase in Lowe syndrome affects actin polymerization. Am J Hum Genet. 2002;71:1420–7. [PMC free article: PMC378584] [PubMed: 12428211]
  • Tosetto E, Addis M, Caridi G, Meloni C, Emma F, Vergine G, Stringini G, Papalia T, Barbano G, Ghiggeri GM, Ruggeri L, Miglietti N, D'Angelo A, Melis MA, Anglani F. Locus heterogeneity of Dent's disease: OCRL1 and TMEM27 genes in patients with no CLCN5 mutations. Pediatr Nephrol. 2009;24:1967–73. [PubMed: 19582483]
  • Ungewickell A, Ward ME, Ungewickell E, Majerus PW. The inositol polyphosphate 5-phosphatase Ocrl associates with endosomes that are partially coated with clathrin. Proc Natl Acad Sci U S A. 2004;101:13501–6. [PMC free article: PMC518786] [PubMed: 15353600]
  • Vicinanza M, Di Campli A, Polishchuk E, Santoro M, Di Tullio G, Godi A, Levtchenko E, De Leo MG, Polishchuk R, Sandoval L, Marzolo MP, De Matteis MA. OCRL controls trafficking through early endosomes via PtdIns4,5P2-dependent regulation of endosomal actin. EMBO J. 2011;30:4970–85. [PMC free article: PMC3242071] [PubMed: 21971085]
  • Warner BE, Inward CD, Burren CP. Gonadotrophin abnormalities in an infant with Lowe syndrome. Endocrinol Diabetes Metab Case Rep. 2017 Apr 19;:2017. [PMC free article: PMC5409933] [PubMed: 28469921]
  • Zaniew M, Bökenkamp A, Kolbuc M, La Scola C, Baronio F, Niemirska A, Szczepanska M, Burger J, La Manna A, Miklaszewska M, Rogowsha-Kalisz A, Gellermann J, Zampetoglou A, Wasilewska A, Roszak M, Moczko J, Krzemien A, Runowski D, Siten G, Zaluska-Lesniewska I, Fonduli P, Zurrida F, Paglialonga F, Gucev Z, Paripovic D, Rus R, Said-Conti V, Sartz L, Chung WY, Park SJ, Lee JW, Park YH, Ahn YH, Sikora P, Stefanidis CJ, Tasic V, Konrad M, Anglani F, Addis M, Cheong HI, Ludwig M, Bockehauer D. Long-term renal outcome in children with OCRL mutations: retrospective analysis of a large international cohort. Nephrol Dial Transplant. 2018;33:85–94. [PubMed: 27708066]
  • Zhang X, Hartz PA, Philip E, Racusen LC, Majerus PW. Cell lines from kidney proximal tubules of a patient with Lowe syndrome lack OCRL inositol polyphosphate 5-phosphatase and accumulate phosphatidylinositol 4,5-bisphosphate. J Biol Chem. 1998;273:1574–82. [PubMed: 9430698]
  • Zhang X, Jefferson AB, Auethavekiat V, Majerus PW. The protein deficient in Lowe syndrome is a phosphatidylinositol-4,5- bisphosphate 5-phosphatase. Proc Natl Acad Sci U S A. 1995;92:4853–6. [PMC free article: PMC41805] [PubMed: 7761412]

Chapter Notes

Author History

Eileen D Brewer, MD (2007-present)
Richard A Lewis, MD, MS (2007-present)
Robert L Nussbaum, MD (2007-present)
Rebecca S Wappner, MD, FAAP, FACMG; Indiana University School of Medicine (2001-2007)

Revision History

  • 18 April 2019 (ha) Comprehensive update posted live
  • 23 February 2012 (me) Comprehensive update posted live
  • 12 March 2008 (cd) Revision: FISH analysis available on a clinical basis
  • 16 November 2007 (cd) Revision: mutation scanning no longer available on a clinical basis
  • 5 January 2007 (me) Comprehensive update posted live
  • 19 September 2003 (me) Comprehensive update posted live
  • 24 July 2001 (me) Review posted live
  • 13 April 2001 (rw) Original submission
Copyright © 1993-2024, University of Washington, Seattle. GeneReviews is a registered trademark of the University of Washington, Seattle. All rights reserved.

GeneReviews® chapters are owned by the University of Washington. Permission is hereby granted to reproduce, distribute, and translate copies of content materials for noncommercial research purposes only, provided that (i) credit for source (http://www.genereviews.org/) and copyright (© 1993-2024 University of Washington) are included with each copy; (ii) a link to the original material is provided whenever the material is published elsewhere on the Web; and (iii) reproducers, distributors, and/or translators comply with the GeneReviews® Copyright Notice and Usage Disclaimer. No further modifications are allowed. For clarity, excerpts of GeneReviews chapters for use in lab reports and clinic notes are a permitted use.

For more information, see the GeneReviews® Copyright Notice and Usage Disclaimer.

For questions regarding permissions or whether a specified use is allowed, contact: ude.wu@tssamda.

Bookshelf ID: NBK1480PMID: 20301653
GeneReviews by Title

Views

  • PubReader
  • Print View
  • Cite this Page
  • PDF version of this page (542K)

In this GeneReview

Bulk Download

GeneReviews Links

Tests in GTR by Gene

Related information

  • MedGen
    Related information in MedGen
  • OMIM
    Related OMIM records
  • PMC
    PubMed Central citations
  • PubMed
    Links to PubMed
  • Gene
    Locus Links

Similar articles in PubMed

See reviews...See all...

Recent Activity

ClearTurn OffTurn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...