Kufor-Rakeb syndrome (KRS) is a rare genetic neurodegenerative disorder characterized by juvenile Parkinsonism, pyramidal degeneration (dystonia), supranuclear palsy, and cognitive impairment. The disease is MONDO_0011706 (Kufor-Rakeb syndrome). Also known as: Kufor Rakeb Syndrome, PARK9, autosomal recessive Parkinson disease 9, autosomal recessive juvenile onset Parkinson disease 9.