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Autosomal recessive hereditary congenital aplasia of the vasa deferentia in four siblings.

作者信息

Schellen T M, van Straaten A

出版信息

Fertil Steril. 1980 Oct;34(4):401-4. doi: 10.1016/s0015-0282(16)45030-2.

DOI:10.1016/s0015-0282(16)45030-2
PMID:7418895
Abstract

Congential absence of the vas deferens is a frequently occurring cause of infertility. Such a disorder can be accompanied by renal agenesis and therefore pyelography should be performed. That such a disorder in man could have genetic aspects has not been mentioned in the literature, but there are reports that this disorder is hereditary in some animals. A family of nine children is described in which four of the five sons were infertile as a result of congenital aplasia of the vasa deferentia. Since there was no evidence that these men had cystic fibrosis and since they did not have the mosaic form of Klinefelter's syndrome, an unrelated developmental defect is postulated. The genetic aspects are discussed and the conclusion is made that the inheritance pattern most probably is autosomal recessive. Finally, the therapeutic problems are discussed. At this time, surgical treatment of this disorder is not encouraging.

摘要

相似文献

1
Autosomal recessive hereditary congenital aplasia of the vasa deferentia in four siblings.
Fertil Steril. 1980 Oct;34(4):401-4. doi: 10.1016/s0015-0282(16)45030-2.
2
Congenital aplasia of the vasa deferentia of autosomal recessive inheritance in two unrelated sib-pairs.
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Three cases of Klinefelter's syndrome with unilateral absence of vas deferens.三例克兰费尔特综合征合并单侧输精管缺如。
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Congenital absence of the vasa deferentia presenting with infertility.先天性输精管缺如伴不育症。
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Men with congenital absence of the vas deferens often have seminal vesicles.先天性输精管缺如的男性通常有精囊。
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The molecular basis of partial penetrance of splicing mutations in cystic fibrosis.囊性纤维化中剪接突变部分外显率的分子基础。
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Congenital bilateral absence of the vas deferens and cystic fibrosis. A genetic commonality.先天性双侧输精管缺如与囊性纤维化。一种遗传共性。
World J Urol. 1993;11(2):82-8. doi: 10.1007/BF00182034.
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CFTR gene variant for patients with congenital absence of vas deferens.先天性输精管缺如患者的CFTR基因变异体
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Congenital aplasia of the vasa deferentia of autosomal recessive inheritance in two unrelated sib-pairs.
Hum Genet. 1985;70(3):288. doi: 10.1007/BF00273461.