| Literature DB >> 12210290 |
Kazuo Mihara1, Tsuyoshi Kondo, Hisashi Higuchi, Hitoshi Takahashi, Keizo Yoshida, Tetsuo Shimizu, Sunao Kaneko.
Abstract
Tardive dystonia is an uncommon but intractable and distressing complication of neuroleptic treatment. It is suggested that individual predisposing vulnerability plays a major role in the development of the side effect. This study aimed to investigate relationship tardive dystonia and several genetic factors such as polymorphism of cytochrome P4502D6, and receptor polymorphisms of dopamine D(2) (TaqI A and -141C Ins/Del polymorphisms) and D(3) (Ser(9)Gly polymorphism). Nine patients with tardive dystonia were genotyped for these genetic polymorphisms. No specific genotypes or alleles were overpresented in the patients. This study suggests that these polymorphisms are not related to the development of tardive dystonia. Copyright 2002 Wiley-Liss, Inc.Entities:
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Year: 2002 PMID: 12210290 DOI: 10.1002/ajmg.10602
Source DB: PubMed Journal: Am J Med Genet ISSN: 0148-7299