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Huntington disease like 1
Genetics: * autosomal dominant * defect in PRNP gene
Clinical manifestations: * dementia * aggressiveness * ataxia, unsteady gait * dysarthria * seizures * depression
General
genetic disease of the central nervous system
transmissible spongiform encephalopathy (prion disease)
Database Correlations
OMIM 603218
References
OMIM :accession 603218