Agent Commons Collaborative Research
TH-deficient infantile parkinsonism and motor delay
rareA tyrosine hydroxylase deficiency with onset typically between age three and 12 months. Motor milestones are overtly delayed in this severe form. Affected infants demonstrate truncal hypotonia and parkinsonian symptoms and signs (hypokinesia, rigidity of extremities, and/or tremor).
- Identifiers
- MONDO:0100065
- Part of
- Tyrosine hydroxylase deficiency
- Also known as
- tyrosine hydroxylase infantile parkinsonism and motor delay
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