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Unilateral partial deferential agenesia and CFTR gene composite heterozygoty (DeltaF508/V938G)

机译:单侧部分差异性不育和CFTR基因复合杂合性(DeltaF508 / V938G)

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This is a case report of a thirty-year-old-man consulting for a primary infertility that was diagnosed four years ago. Andrologic exam was normal. Two spermograms found normal spermatic parameters. An uro-genital echography with a RMI showed that a unilateral agenesia of the left vas deferens in the pelvic portion. Then, a composite heterozygoty of the CFTR gene (DeltaF508/V938G) was found. This is the first time that the association of these two mutations has been described. This case also makes it possible to wonder about the need for realizing, or not, a systematic basis imagery (ultrasound examination in first), in the event of infertility of the couple. In this context, the discovery of an echographic anomaly made it possible to identify CFTR mutations, whose physiopathological implication in the infertility can be discussed (CFTR related disorders)...
机译:这是四年前诊断为原发性不孕症的一名30岁男子咨询的病例报告。男科检查正常。两个精子图发现正常的精子参数。带有RMI的尿生殖器超声检查显示,盆腔部分左侧输精管有单侧发育不全。然后,发现了CFTR基因的复合杂合子(DeltaF508 / V938G)。这是第一次描述这两个突变的关联。这种情况还使人们可能会怀疑,如果夫妻不育,是否需要实现系统的基础图像(首先是超声检查)。在这种情况下,超声回波图异常的发现使我们有可能识别CFTR突变,可以讨论其在不育症中的生理病理学意义(CFTR相关疾病)...

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