## Abstract This is the first reported case of dystonia with a partial deletion of the long arm (q) of chromosome 18. Neurologic findings in the 18qβ syndrome include mental retardation, seizures, nystagmus, incoordination, tremor, and chorea. A 36βyearβold woman with an 18q terminal deletion [Kary
Dystonia in a patient with deletion of 18p
β Scribed by F. Tezzon; T. Zanoni; M. G. Passarin; G. Ferrari
- Publisher
- Springer Milan
- Year
- 1998
- Tongue
- English
- Weight
- 526 KB
- Volume
- 19
- Category
- Article
- ISSN
- 1590-1874
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