| Literature DB >> 8684395 |
C Klein1, G K Wenning, N P Quinn, C D Marsden.
Abstract
We report a nonconsanguineous family in whom two (of three) sons developed isolated chorea in early childhood, suggesting a diagnosis of benign hereditary chorea (BHC). However, cerebellar ataxia and oculomotor apraxia, without telangiectasia, subsequently developed. Chromosome analysis showed increased radiosensitivity in both brothers and translocations in the younger one. We conclude that ataxia with chromosomal instability may masquerade as BHC in some patients.Entities:
Mesh:
Year: 1996 PMID: 8684395 DOI: 10.1002/mds.870110217
Source DB: PubMed Journal: Mov Disord ISSN: 0885-3185 Impact factor: 10.338