Literature DB >> 12210290

Tardive dystonia and genetic polymorphisms of cytochrome P4502D6 and dopamine D2 and D3 receptors: a preliminary finding.

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.

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Year:  2002        PMID: 12210290     DOI: 10.1002/ajmg.10602

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  6 in total

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5.  Tardive oculogyric crisis during treatment with clozapine: report of three cases.

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Review 6.  Genetic Testing for Antipsychotic Pharmacotherapy: Bench to Bedside.

Authors:  Mujeeb U Shad
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  6 in total

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