Literature DB >> 7418895

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

T M Schellen, A van Straaten.   

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.

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Year:  1980        PMID: 7418895     DOI: 10.1016/s0015-0282(16)45030-2

Source DB:  PubMed          Journal:  Fertil Steril        ISSN: 0015-0282            Impact factor:   7.329


  5 in total

1.  CFTR gene variant for patients with congenital absence of vas deferens.

Authors:  J Zielenski; P Patrizio; M Corey; B Handelin; D Markiewicz; R Asch; L C Tsui
Journal:  Am J Hum Genet       Date:  1995-10       Impact factor: 11.025

2.  Congenital aplasia of the vasa deferentia of autosomal recessive inheritance in two unrelated sib-pairs.

Authors:  A Czeizel
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

3.  The molecular basis of partial penetrance of splicing mutations in cystic fibrosis.

Authors:  N Rave-Harel; E Kerem; M Nissim-Rafinia; I Madjar; R Goshen; A Augarten; A Rahat; A Hurwitz; A Darvasi; B Kerem
Journal:  Am J Hum Genet       Date:  1997-01       Impact factor: 11.025

Review 4.  Congenital bilateral absence of the vas deferens and cystic fibrosis. A genetic commonality.

Authors:  R D Oates; J A Amos
Journal:  World J Urol       Date:  1993       Impact factor: 4.226

Review 5.  Heterogeneity in the severity of cystic fibrosis and the role of CFTR gene mutations.

Authors:  M Dean; G Santis
Journal:  Hum Genet       Date:  1994-04       Impact factor: 4.132

  5 in total

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