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6号染色体单亲二体与短暂性新生儿糖尿病

Paternal uniparental disomy of chromosome 6 and transient neonatal diabetes mellitus.

作者信息

Gardner R J, Robinson D O, Lamont L, Shield J P, Temple I K

机构信息

Wessex Regional Genetics Laboratory, Salisbury District Hospital, Wiltshire, UK.

出版信息

Clin Genet. 1998 Dec;54(6):522-5. doi: 10.1111/j.1399-0004.1998.tb03774.x.

Abstract

Transient neonatal diabetes mellitus occurs in growth-retarded infants, has an incidence of 1 in 400000 live births and has been associated with both paternal uniparental disomy of chromosome 6 and paternal duplications of 6q. We analysed samples from our cohort of patients with transient neonatal diabetes mellitus for uniparental disomy of chromosome 6 using polymorphic microsatellite repeat analysis. We report here the fifth case of paternal uniparental disomy of chromosome 6 associated with classic transient neonatal diabetes mellitus and estimate that uniparental disomy of chromosome 6 accounts for approximately one fifth of cases of transient neonatal diabetes mellitus.

摘要

短暂性新生儿糖尿病发生于生长发育迟缓的婴儿中,活产婴儿中的发病率为1/400000,且与6号染色体的父源性单亲二体性以及6q的父源性重复有关。我们使用多态性微卫星重复分析,对我们的短暂性新生儿糖尿病患者队列样本进行了6号染色体单亲二体性分析。我们在此报告第5例与经典短暂性新生儿糖尿病相关的6号染色体父源性单亲二体性病例,并估计6号染色体单亲二体性约占短暂性新生儿糖尿病病例的五分之一。

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