AZFb y染色体微缺失从父亲自然传播给他的三个儿子。

H Samli, M Murat Samli, M Solak
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引用次数: 10

摘要

Y染色体长臂(Yq)上所谓的无精子症因子(AZF)位点的微缺失是严重少精症或无精子症的病因。除非使用辅助生殖技术,否则患者无法生育。我们报告一例无精子患者(先证者)和三个兄弟谁继承了一个Yq微缺失从他们的父亲通过自然怀孕。使用市售试剂盒提取白细胞DNA。共筛选了15对基于序列标记位点(STSs)的引物,涵盖AZFa、b和c区。所有兄弟和他们的父亲都携带rna结合基序(RBM)基因所在的AZFb亚区Yq微缺失。先证者携带AZFa和AZFb亚区额外的缺失。RBM缺失可能与少精症有关,允许自然受孕,因此自然传播这种遗传异常。
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Natural transmission of AZFb Y-chromosomal microdeletion from father to his three sons.

Microdeletions of the so-called azoospermia factor (AZF) locus of the Y chromosome long arm (Yq) are an etiological factor of severe oligozoospermia or azoospermia. Patients affected are infertile unless assisted reproductive techniques are used. We report the case of an azoospermic patient (proband) and three brothers who inherited a Yq microdeletion from their father through a spontaneous pregnancy. Leukocyte DNA was extracted using a commercially available kit. A total of 15 pairs of sequence-tagged site (STSs) based primers, spanning the AZFa, b and c regions, were used for screening. All brothers and their father carried a Yq microdeletion of the AZFb subregion where the RNA-binding motif (RBM) gene is located. The proband carried additional deletions of the AZFa and AZFb subregions. RBM deletion can be associated with oligozoospermia allowing natural conception and therefore natural transmission of this genetic anomaly.

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