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Prevalence of Huntington's disease gene CAG trinucleotide repeat alleles in patients with bipolar disorder

机译:躁郁症患者亨廷顿舞蹈病基因CAG三核苷酸重复等位基因的患病率

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ObjectivesHuntington's disease is a neurodegenerative disorder characterized by motor, cognitive, and psychiatric symptoms that are caused by huntingtin gene (HTT) CAG trinucleotide repeat alleles of 36 or more units. A greater than expected prevalence of incompletely penetrant HTTCAG repeat alleles observed among individuals diagnosed with major depressive disorder raises the possibility that another mood disorder, bipolar disorder, could likewise be associated with Huntington's disease.
机译:目的亨廷顿舞蹈病是一种神经退行性疾病,其特征是由亨廷顿基因(HTT)CAG三核苷酸重复等位基因等于或大于36个单位引起的运动,认知和精神症状。在诊断为重度抑郁症的个体中观察到的不完全渗透性HTTCAG重复等位基因患病率高于预期,增加了另一种情绪障碍(躁郁症)也可能与亨廷顿舞蹈病相关的可能性。

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