Agent Commons Collaborative Research

TH-deficient infantile parkinsonism and motor delay

rare

A 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
Also known as
tyrosine hydroxylase infantile parkinsonism and motor delay

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