Autosomal recessive Parkinson disease 14
MONDO:0013060A 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.
Also known as: PARK14, PLA2G6 hereditary late onset Parkinson disease, PLA2G6-related dystonia-parkinsonism, autosomal recessive Parkinson disease type 14, dystonia-parkinsonism, Paisan-Ruiz type, hereditary late onset Parkinson disease caused by mutation in PLA2G6, Parkinson disease 14, autosomal recessive, adult-onset dystonia - parkinsonism
25 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive Parkinson disease 14 itself.
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