Autosomal recessive juvenile Parkinson disease 2

A group of disorders which feature impaired motor control characterized by bradykinesia, muscle rigidity; tremor; and postural instability. Parkinsonian diseases are generally divided into primary parkinsonism (see Parkinson disease), secondary parkinsonism (see Parkinson disease, secondary) and inherited forms. These conditions are associated with dysfunction of dopaminergic or closely related motor integration neuronal pathways in the basal ganglia.

Also known as: PRKN young-onset Parkinson disease, Parkinson disease, juvenile, type 2, autosomal recessive juvenile Parkinson disease 2, autosomal recessive juvenile Parkinson disease type 2, young-onset Parkinson disease caused by mutation in PRKN, JP, PARK2, PDJ

14 clinical trials for this condition and its sub-types, 2 tagged with Autosomal recessive juvenile Parkinson disease 2 itself.