Bruxism in Huntington's disease
β Scribed by Elan D. Louis; Elizabeth Tampone
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- English
- Weight
- 13 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0885-3185
- DOI
- 10.1002/mds.1129
No coin nor oath required. For personal study only.
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Huntington's disease (HD) is a late-onset degenerative disorder of the central nervous system, caused by a dominantly inherited mutation in a gene on chromosome 4p. The identification of the trinucleotide repeat mutation responsible for this disorder has been an important step towards understanding
## Abstract The authors report a patient with Huntington's disease (HD) presenting with severe chorea. The motor scale of the unified HD rating scale (UHDRSβI) revealed 81 points. Motor function clearly improved with zotepine, until she reached an UHDRSβI of 34 points on day 7 of treatment. The pat
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Two brothers with clinically definite adult Huntington's disease developed disabling myoclonus years after the first signs of the disease. Their electroencephalograms were consistent with a primary generalized epilepsy, although neither man had seizures. The myoclonus was controlled with valproic ac