Kufor-Rakeb syndrome

MONDO:0011706

Kufor-Rakeb syndrome (KRS) is a rare genetic neurodegenerative disorder characterized by juvenile Parkinsonism, pyramidal degeneration (dystonia), supranuclear palsy, and cognitive impairment.

Also known as: Kufor Rakeb Syndrome, Kufor-Rakeb syndrome, PARK9, KRPPD, KRS, Pallidopyramidal Degeneration with supranuclear upgaze paresis and dementia, Pallidopyramidal degeneration with supranuclear upgaze paresis, and dementia, Parkinson disease 9, autosomal recessive

199 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Sub-types

Broader categories

Sort by