Huntington disease like 1

Genetics

* autosomal dominant * defect in PRNP gene

Clinical manifestations

* dementia * aggressiveness * ataxia, unsteady gait * dysarthria * seizures * depression

More general terms

• transmissible spongiform encephalopathy (prion disease)
• genetic disease of the central nervous system

Database

• OMIM: https://mirror.omim.org/entry/603218