Macrocephaly/megalencephaly syndrome, autosomal recessive
- Synonyms
- Fryns Dereymaeker Haegeman syndrome
Summary
Available tests
Clinical tests (5 available)
Clinical features
Help- Abnormality of head or neck
- Broad forehead
Broad forehead
- MedGen UID: 338610
- Concept ID: C1849089
- Finding: Finding
Abnormality of head or neck
- Coarse facial features
Coarse facial features
- MedGen UID: 335284
- Concept ID: C1845847
- Finding: Finding
Abnormality of head or neck
- Mandibular prognathia
Mandibular prognathia
- MedGen UID: 98316
- Concept ID: C0399526
- Finding: Finding
Abnormality of head or neck
- Pointed chin
Pointed chin
- MedGen UID: 336193
- Concept ID: C1844505
- Finding: Finding
Abnormality of head or neck
- Broad forehead
- Abnormality of limbs
- Genu valgum
Genu valgum
- MedGen UID: 154364
- Concept ID: C0576093
- Finding: Anatomical Abnormality
Abnormality of limbs
- Patellar subluxation
Patellar subluxation
- MedGen UID: 163635
- Concept ID: C0857276
- Finding: Pathologic Function
Abnormality of limbs
- Genu valgum
- Abnormality of the endocrine system
- Adrenal medullary hypoplasia
Adrenal medullary hypoplasia
- MedGen UID: 870276
- Concept ID: C4024717
- Finding: Finding
Abnormality of the endocrine system
- Adrenal medullary hypoplasia
- Abnormality of the eye
- Astigmatism
Astigmatism
- MedGen UID: 2473
- Concept ID: C0004106
- Finding: Disease or Syndrome
Abnormality of the eye
- Myopia
Myopia
- MedGen UID: 44558
- Concept ID: C0027092
- Finding: Disease or Syndrome
Abnormality of the eye
- Optic atrophy
Optic atrophy
- MedGen UID: 18180
- Concept ID: C0029124
- Finding: Disease or Syndrome
Abnormality of the eye
- Strabismus
Strabismus
- MedGen UID: 21337
- Concept ID: C0038379
- Finding: Disease or Syndrome
Abnormality of the eye
- Astigmatism
- Abnormality of the genitourinary system
- Calcium oxalate urolithiasis
Calcium oxalate urolithiasis
- MedGen UID: 318935
- Concept ID: C1833683
- Finding: Disease or Syndrome
Abnormality of the genitourinary system
- Calcium oxalate urolithiasis
- Abnormality of the immune system
- Celiac disease
Celiac disease
- MedGen UID: 3291
- Concept ID: C0007570
- Finding: Disease or Syndrome
Abnormality of the immune system
- Celiac disease
- Abnormality of the musculoskeletal system
- Dolichocephaly
Dolichocephaly
- MedGen UID: 65142
- Concept ID: C0221358
- Finding: Congenital Abnormality
Abnormality of the musculoskeletal system
- Isolated scaphocephaly
Isolated scaphocephaly
- MedGen UID: 82712
- Concept ID: C0265534
- Finding: Congenital Abnormality
Abnormality of the musculoskeletal system
- Macrocephaly
Macrocephaly
- MedGen UID: 745757
- Concept ID: C2243051
- Finding: Finding
Abnormality of the musculoskeletal system
- Dolichocephaly
- Abnormality of the nervous system
- Delayed speech and language development
Delayed speech and language development
- MedGen UID: 105318
- Concept ID: C0454644
- Finding: Finding
Abnormality of the nervous system
- Depression
Depression
- MedGen UID: 4229
- Concept ID: C0011581
- Finding: Mental or Behavioral Dysfunction
Abnormality of the nervous system
- Global developmental delay
Global developmental delay
- MedGen UID: 107838
- Concept ID: C0557874
- Finding: Finding
Abnormality of the nervous system
- Hydrocephalus
Hydrocephalus
- MedGen UID: 9335
- Concept ID: C0020255
- Finding: Disease or Syndrome
Abnormality of the nervous system
- Intellectual disability
Intellectual disability
- MedGen UID: 811461
- Concept ID: C3714756
- Finding: Mental or Behavioral Dysfunction
Abnormality of the nervous system
- Intellectual disability, mild
Intellectual disability, mild
- MedGen UID: 10044
- Concept ID: C0026106
- Finding: Mental or Behavioral Dysfunction
Abnormality of the nervous system
- Megalencephaly
Megalencephaly
- MedGen UID: 65141
- Concept ID: C0221355
- Finding: Congenital Abnormality
Abnormality of the nervous system
- Psychotic disorder
Psychotic disorder
- MedGen UID: 19568
- Concept ID: C0033975
- Finding: Mental or Behavioral Dysfunction
Abnormality of the nervous system
- Thick corpus callosum
Thick corpus callosum
- MedGen UID: 371993
- Concept ID: C1835194
- Finding: Finding
Abnormality of the nervous system
- Delayed speech and language development
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