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