MeSH Browser

MeSH Supplementary: Kufor-Rakeb syndrome
Unique ID: C537177
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537177
Entry Term(s): KRPPD Kufor Rakeb pallidopyramidal degeneration with supranuclear upgaze paresis and dementia; Pallidopyramidal Degeneration with Supranuclear Upgaze Paresis and Dementia; Parkinson disease 9
Registry Numbers: 0
Heading Mapped to: *Parkinsonian Disorders
Frequency: 40
Note: A rare autosomal recessive form of juvenile-onset atypical Parkinson disease (PARK9) associated with supranuclear gaze palsy, SPASTICITY, and DEMENTIA. Some patients have neuroradiologic evidence of iron deposition in the BASAL GANGLIA. Mutations in the ATP13A2 gene have been identified. OMIM: 606693
Date of Entry: 2010/08/25
Revision Date: 2019/06/19

Kufor-Rakeb syndrome MeSH Supplementary Concept Data 2025