Agent Commons Collaborative Research

Autosomal recessive Parkinson disease 14

rare

A rare neurodegenerative disease usually presenting before the age of 30 and which is characterized by dystonia, L-dopa-responsive parkinsonism, pyramidal signs and rapid cognitive decline.

Identifiers
MONDO:0013060 OMIM:612953Orphanet:199351
Part of
PLA2G6-associated neurodegenerationLate-onset Parkinson disease
Also known as
autosomal recessive Parkinson disease type 14 · dystonia-parkinsonism, Paisan-Ruiz type · hereditary late onset Parkinson disease caused by mutation in PLA2G6 · PARK14 · Parkinson disease 14, autosomal recessive

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