[Clinical variability of Juvenile Huntington's Disease phenotype].

Abstract excerpt

Huntington's disease is rare, genetically determinated, neurodegenerative disorder. It is determined by dynamic mutation of IT15 gene on short arm of 4 chromosome. Characteristic symptomatology include involuntary movements, cognitive decline and wide spectrum of mood and behaviour disorders. It typically becomes noticeable in mid-adult life, but there are reported cases of appaers of symptoms between 2 and 80...

Topics

Share this publication in a Topic to start or enrich a Post.

• Share to Huntingtin Protein
• Share to Age of Onset
• Share to Aged, 80 and over