Huntington's Disease¶
Walker, F. O. (2007). Huntington's Disease.
Cited by¶
1 citation across 1 artifact.
Each citation links to the sentence it supports in the citing article.
Domain-specific¶
- Ostrich Effect
- Huntington's is a late-onset, currently incurable neurodegenerative disorder, and a definitive predictive test has been available since the early 1990s for people with an affected parent (who each carry a 50% prior risk).
This sourceA clinical review describing Huntington’s disease as an autosomal-dominant, progressive neurodegenerative disorder whose symptoms typically begin in middle age.
Supported in partVerified against a saved copy of the source
“Huntington's disease is an autosomal-dominant, progressive neurodegenerative disorder with a distinct phenotype, including chorea and dystonia, incoordination, cognitive decline, and behavioural difficulties. ... Typically, onset of symptoms is in middle-age after affected individuals have had children”
- Huntington's is a late-onset, currently incurable neurodegenerative disorder, and a definitive predictive test has been available since the early 1990s for people with an affected parent (who each carry a 50% prior risk).
Verification¶
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Registry ID ref:5dfadba4afb9 · see in the full table