| Literature DB >> 8871591 |
S B Bressman1, T T Warner, L Almasy, R J Uitti, P E Greene, G A Heiman, D Raymond, B Ford, D de Leon, S Fahn, P L Kramer, N J Risch, D M Maraganore, T G Nygaard, A E Harding.
Abstract
Clinical-genetic studies of idiopathic torsion dystonia (ITD) indicate that the DYT1 gene on chromosome 9q34 is responsible for most childhood limb-onset disease. The genetic basis of adult-onset ITD is less well studied. In most multiplex adult-onset ITD families, dystonia is limited to the cervical, cranial, or brachial muscles; in a few rare families, dystonia also involves the legs and trunk. Previous linkage studies have excluded the DYT1 locus in these atypical families. We studied two large non-Jewish families with adult-onset ITD limited to the cervical and brachial muscles and excluded the DYT1-containing region. This study further restricts the role of DYT1 to childhood limb-onset ITD and suggests that other genes are responsible for focal adult-onset ITD.Entities:
Mesh:
Year: 1996 PMID: 8871591 DOI: 10.1002/ana.410400421
Source DB: PubMed Journal: Ann Neurol ISSN: 0364-5134 Impact factor: 10.422