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Parkinsonian-pyramidal syndrome

ORPHA:171695· ICD-10 G20

Definition

Parkinsonian-pyramidal syndrome is a rare, genetic, neurological disorder characterized by the association of both parkinsonian (i.e. bradykinesia, rigidity and/or rest tremor) and pyramidal (i.e. increased reflexes, extensor plantar reflexes, pyramidal weakness or spasticity) manifestations, which vary according to the underlying associated disease (e.g. neurodegenerative disease, inborn errors of metabolism).

Inheritance
Autosomal recessive
Age of onset
Adolescent, Adult