| Literature DB >> 2966545 |
Abstract
Huntington's disease is characterized by striatal degeneration, leading to progressive choreoathetoid movements, dementia and behavioral changes. It is inherited as an autosomal dominant illness with complete penetrance. New technology has localized the aberrant gene, and presymptomatic and even prenatal testing may eventually be available. Although no definitive treatment currently exists, judicious use of neuroleptics, appropriate referrals and a strong therapeutic alliance with the family may be helpful.Entities:
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Year: 1988 PMID: 2966545
Source DB: PubMed Journal: Am Fam Physician ISSN: 0002-838X Impact factor: 3.292