The causes of sporadic and ‘senile’ chorea
✍ Scribed by Warren, J. D. ;Firgaira, F. ;Thompson, E. M. ;Kneebone, C. S. ;Blumbergs, P. C. ;Thompson, P. D.
- Book ID
- 108999918
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 269 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0004-8291
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## Abstract Senile chorea, a late‐onset, slowly progressive disorder without mental changes, is a poorly characterized entity. It is often thought to represent late‐onset Huntington's disease in which the chorea precedes the mental changes and the family history is absent due to parental death befo
## Abstract Benign hereditary chorea (BHC; OMIM 118700) is an autosomal dominant movement disorder. Mutations in the thyroid transcription factor 1 (TITF1) gene have been linked with BHC. The phenotype for BHC is highly variable and may include atypical features such as dystonia, slow saccades, and