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

25 clinical trials for this condition and its sub-types, 0 tagged with Kufor-Rakeb syndrome itself.

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↑ Neurodegeneration with brain iron accumulation (8) ↑ Juvenile-onset Parkinson disease (0)

Sub-types of Kufor-Rakeb syndrome

Parkinsonism due to ATP13A2 deficiency 0 trials

Including sub-types (25) Tagged with Kufor-Rakeb syndrome (0)

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