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Dysbindin (DTNBP1, 6p22.3) is associated with childhood-onset psychosis and endophenotypes measured by the Premorbid Adjustment Scale (PAS).
Gornick, M C; Addington, A M; Sporn, A; Gogtay, N; Greenstein, D; Lenane, M; Gochman, P; Ordonez, A; Balkissoon, R; Vakkalanka, R; Weinberger, D R; Rapoport, J L; Straub, R E.
Afiliação
  • Gornick MC; Child Psychiatry Branch, IRP, National Institute of Mental Health, NIH, Bethesda, MD 20892-1600, USA.
J Autism Dev Disord ; 35(6): 831-8, 2005 Dec.
Article em En | MEDLINE | ID: mdl-16283082
ABSTRACT
Straub et al. (2002) recently identified the 6p22.3 gene dysbindin (DTNBP1) through positional cloning as a schizophrenia susceptibility gene. We studied a rare cohort of 102 children with onset of psychosis before age 13. Standardized ratings of early development, medication response, neuropsychological and cognitive performance, premorbid dysfunction and clinical follow-up were obtained. Fourteen SNPs were genotyped in the gene DTNBP1. Family-based pairwise and haplotype transmission disequilibrium test (TDT) analysis with the clinical phenotype, and quantitative transmission disequilibrium test (QTDT) explored endophenotype relationships. One SNP was associated with diagnosis (TDT p=.01). The QTDT analyses showed several significant relationships. Four adjacent SNPs were associated (p values=.0009-.003) with poor premorbid functioning. These findings support the hypothesis that this and other schizophrenia susceptibility genes contribute to early neurodevelopmental impairment.
Assuntos
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Base de dados: MEDLINE Assunto principal: Fenótipo / Transtornos Psicóticos / Esquizofrenia / Ajustamento Social / Cromossomos Humanos Par 6 / Proteínas de Transporte / Inquéritos e Questionários Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Child / Humans Idioma: En Ano de publicação: 2005 Tipo de documento: Article
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Base de dados: MEDLINE Assunto principal: Fenótipo / Transtornos Psicóticos / Esquizofrenia / Ajustamento Social / Cromossomos Humanos Par 6 / Proteínas de Transporte / Inquéritos e Questionários Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Child / Humans Idioma: En Ano de publicação: 2005 Tipo de documento: Article