Autosomal recessive DOPA responsive dystonia
- Synonyms
- Autosomal Recessive Infantile Parkinsonism; DYT-TH; Segawa syndrome, autosomal recessive; TH-deficient dopa-responsive dystonia; Tyrosine Hydroxylase-Deficient Dopa-Responsive Dystonia
- Modes of inheritance
- Autosomal recessive inheritance (Orphanet)
Summary
Excerpted from the GeneReview:- Full text of GeneReview (by section):
- Summary
- GeneReview Scope
- Diagnosis
- Clinical Characteristics
- Genetically Related (Allelic) Disorders
- Differential Diagnosis
- Management
- Genetic Counseling
- Resources
- Molecular Genetics
- Chapter Notes
- References
- Authors:
- Yoshiaki Furukawa
- Stephen Kish
- view full author information
Available tests
Check Related conditions for additional relevant tests.
Clinical tests (80 available)
Biochemical Genetics Tests
Clinical features
Help- Abnormality of head or neck
- Mask-like facies
Mask-like facies
- MedGen UID: 140860
- Concept ID: C0424448
- Finding: Finding
Abnormality of head or neck
- Mask-like facies
- 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
- Rigidity
Rigidity
- MedGen UID: 7752
- Concept ID: C0026837
- Finding: Sign or Symptom
Abnormality of the musculoskeletal system
- Axial hypotonia
- Abnormality of the nervous system
- Abnormality of extrapyramidal motor function
Abnormality of extrapyramidal motor function
- MedGen UID: 115941
- Concept ID: C0234133
- Finding: Sign or Symptom
Abnormality of the nervous system
- Decreased CSF homovanillic acid concentration
Decreased CSF homovanillic acid concentration
- MedGen UID: 1813045
- Concept ID: C5676596
- Finding: Finding
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
- Gait ataxia
Gait ataxia
- MedGen UID: 155642
- Concept ID: C0751837
- Finding: Sign or Symptom
Abnormality of the nervous system
- Hypokinesia
Hypokinesia
- MedGen UID: 39223
- Concept ID: C0086439
- Finding: Finding
Abnormality of the nervous system
- Limb dystonia
Limb dystonia
- MedGen UID: 152944
- Concept ID: C0751093
- Finding: Sign or Symptom
Abnormality of the nervous system
- Motor delay
Motor delay
- MedGen UID: 381392
- Concept ID: C1854301
- Finding: Finding
Abnormality of the nervous system
- Myoclonus
Myoclonus
- MedGen UID: 10234
- Concept ID: C0027066
- Finding: Finding
Abnormality of the nervous system
- Parkinsonian disorder
Parkinsonian disorder
- MedGen UID: 66079
- Concept ID: C0242422
- Finding: Disease or Syndrome
Abnormality of the nervous system
- Parkinsonism with favorable response to dopaminergic medication
Parkinsonism with favorable response to dopaminergic medication
- MedGen UID: 375989
- Concept ID: C1846868
- Finding: Disease or Syndrome
Abnormality of the nervous system
- Tremor
Tremor
- MedGen UID: 21635
- Concept ID: C0040822
- Finding: Sign or Symptom
Abnormality of the nervous system
- Abnormality of extrapyramidal motor function
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