Neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia
Summary
Available tests
Clinical tests (3 available)
Molecular Genetics Tests
Clinical features
Help- Abnormality of blood and blood-forming tissues
- Hypochromic anemia
Hypochromic anemia
- MedGen UID: 8065
- Concept ID: C0002884
- Finding: Disease or Syndrome
Abnormality of blood and blood-forming tissues
- Microcytic anemia
Microcytic anemia
- MedGen UID: 1673948
- Concept ID: C5194182
- Finding: Disease or Syndrome
Abnormality of blood and blood-forming tissues
- Hypochromic anemia
- Abnormality of head or neck
- Midface retrusion
Midface retrusion
- MedGen UID: 339938
- Concept ID: C1853242
- Finding: Anatomical Abnormality
Abnormality of head or neck
- Short philtrum
Short philtrum
- MedGen UID: 350006
- Concept ID: C1861324
- Finding: Finding
Abnormality of head or neck
- Midface retrusion
- Abnormality of the digestive system
- Feeding difficulties
Feeding difficulties
- MedGen UID: 65429
- Concept ID: C0232466
- Finding: Finding
Abnormality of the digestive system
- Feeding difficulties
- Abnormality of the eye
- Ptosis
Ptosis
- MedGen UID: 2287
- Concept ID: C0005745
- Finding: Disease or Syndrome
Abnormality of the eye
- Ptosis
- Abnormality of the musculoskeletal system
- Axial hypotonia
Axial hypotonia
- MedGen UID: 342959
- Concept ID: C1853743
- Finding: Finding
Abnormality of the musculoskeletal system
- Hypertonia
Hypertonia
- MedGen UID: 10132
- Concept ID: C0026826
- Finding: Finding
Abnormality of the musculoskeletal system
- Poor head control
Poor head control
- MedGen UID: 322809
- Concept ID: C1836038
- Finding: Finding
Abnormality of the musculoskeletal system
- Axial hypotonia
- Abnormality of the nervous system
- Absent speech
Absent speech
- MedGen UID: 340737
- Concept ID: C1854882
- Finding: Finding
Abnormality of the nervous system
- Babinski sign
Babinski sign
- MedGen UID: 19708
- Concept ID: C0034935
- Finding: Finding
Abnormality of the nervous system
- Bilateral tonic-clonic seizure with generalized onset
Bilateral tonic-clonic seizure with generalized onset
- MedGen UID: 1368929
- Concept ID: C4476643
- Finding: Sign or Symptom
Abnormality of the nervous system
- Cerebral palsy
Cerebral palsy
- MedGen UID: 854
- Concept ID: C0007789
- Finding: Disease or Syndrome
Abnormality of the nervous system
- Cerebral white matter atrophy
Cerebral white matter atrophy
- MedGen UID: 868341
- Concept ID: C4022735
- Finding: Anatomical Abnormality
Abnormality of the nervous system
- Chorea
Chorea
- MedGen UID: 3420
- Concept ID: C0008489
- Finding: Disease or Syndrome
Abnormality of the nervous system
- Choreoathetosis
Choreoathetosis
- MedGen UID: 39313
- Concept ID: C0085583
- Finding: Disease or Syndrome
Abnormality of the nervous system
- Delayed myelination
Delayed myelination
- MedGen UID: 224820
- Concept ID: C1277241
- Finding: Finding
Abnormality of the nervous system
- Dyskinesia
Dyskinesia
- MedGen UID: 8514
- Concept ID: C0013384
- Finding: Disease or Syndrome
Abnormality of the nervous system
- Dystonic disorder
Dystonic disorder
- MedGen UID: 3940
- Concept ID: C0013421
- Finding: Sign or Symptom
Abnormality of the nervous system
- EEG abnormality
EEG abnormality
- MedGen UID: 56235
- Concept ID: C0151611
- Finding: Finding
Abnormality of the nervous system
- Global developmental delay
Global developmental delay
- MedGen UID: 107838
- Concept ID: C0557874
- Finding: Finding
Abnormality of the nervous system
- Hyperreflexia
Hyperreflexia
- MedGen UID: 57738
- Concept ID: C0151889
- Finding: Finding
Abnormality of the nervous system
- Orofacial dyskinesia
Orofacial dyskinesia
- MedGen UID: 57747
- Concept ID: C0152115
- Finding: Disease or Syndrome
Abnormality of the nervous system
- Profound global developmental delay
Profound global developmental delay
- MedGen UID: 766364
- Concept ID: C3553450
- Finding: Disease or Syndrome
Abnormality of the nervous system
- Reduced cerebral white matter volume
Reduced cerebral white matter volume
- MedGen UID: 1815057
- Concept ID: C5706151
- Finding: Finding
Abnormality of the nervous system
- Reduced eye contact
Reduced eye contact
- MedGen UID: 303190
- Concept ID: C1445953
- Finding: Finding
Abnormality of the nervous system
- Seizure
Seizure
- MedGen UID: 20693
- Concept ID: C0036572
- Finding: Sign or Symptom
Abnormality of the nervous system
- Spasticity
Spasticity
- MedGen UID: 7753
- Concept ID: C0026838
- Finding: Sign or Symptom
Abnormality of the nervous system
- Absent speech
- Ear malformation
- Low-set ears
Low-set ears
- MedGen UID: 65980
- Concept ID: C0239234
- Finding: Congenital Abnormality
Ear malformation
- Low-set ears
IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.