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首页> 外文期刊>Cytogenetic and genome research >Familial Translocation t(6;20)(p21;p13) Resulting in Partial Trisomy 6p and Partial Monosomy 20p: Report of a New Case and Review of the Literature
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Familial Translocation t(6;20)(p21;p13) Resulting in Partial Trisomy 6p and Partial Monosomy 20p: Report of a New Case and Review of the Literature

机译:家族易位t(6; 20)(p21; p13)导致部分三体性6p和部分单体性20p:一个新病例的报告和文献复习

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摘要

Carriers of completely balanced chromosomal translocations have all necessary genetic information. Nevertheless, because of the possibility of maldistribution during gametogenesis, they are at increased risk for infertility, miscarriage, stillbirth or having a child with congenital anomalies including mental retardation. As postnatal clinical reports are infrequent, prediction of clinical course for specific unbalanced karyotypes diagnosed during pregnancy remains difficult. Here, we report the 6th case of partial trisomy 6p and partial monosomy 20p due to an unbalanced adjacent-1 segregation of the rare familial translocation t(6;20)(p21;p13). We give a thorough clinical description of the present case, demonstrating broad phenotypic overlap with the 5 previously published cases reviewed here, providing important data on postnatal outcome
机译:完全平衡的染色体易位的载体具有所有必要的遗传信息。然而,由于在配子发生过程中分布不均的可能性,它们的不孕,流产,死产或生有先天异常(包括智力低下)的孩子的风险增加。由于产后临床报告很少,因此对怀孕期间诊断出的特定不平衡核型的临床病程进行预测仍然很困难。在这里,我们报告了第六例部分三体性6p和部分单性20p,这是由于罕见的家族易位t(6; 20)(p21; p13)的不相邻1分离引起的。我们对本病例进行了全面的临床描述,证明与此处回顾的5例先前发表的病例有广泛的表型重叠,提供了有关出生后结局的重要数据

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