Literature DB >> 1632444

Congenital absence of the vas deferens: recurrence in a family.

R A Martin1, K L Jones, E C Downey.   

Abstract

We report on 2 brothers with congenital absence of the vas deferens discovered in childhood during inguinal hernia repairs. The vas is absent unilaterally in one sib and bilaterally in the other. The unusual presentation of inguinal hernias in these children is discussed as well as mechanisms of inheritance and associated risk of renal anomalies.

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Year:  1992        PMID： 1632444     DOI： 10.1002/ajmg.1320420517

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN： 0148-7299


  3 in total

Review 1.  Congenital bilateral absence of the vas deferens as an atypical form of cystic fibrosis: reproductive implications and genetic counseling.

Authors:  D A S de Souza; F R Faucz; L Pereira-Ferrari; V S Sotomaior; S Raskin
Journal:  Andrology       Date:  2017-12-07       Impact factor: 3.842

2.  CFTR haplotype analysis reveals genetic heterogeneity in the etiology of congenital bilateral aplasia of the vas deferens.

Authors:  N Rave-Harel; I Madgar; R Goshen; M Nissim-Rafinia; A Ziadni; A Rahat; O Chiba; Y M Kalman; C Brautbar; D Levinson
Journal:  Am J Hum Genet       Date:  1995-06       Impact factor: 11.025

3.  Congenital unilateral absence of the vas deferens with ipsilateral renal agenesis encountered during laparoscopic totally extraperitoneal inguinal hernia repair in an adult patient: A case report.

Authors:  Karel M Smeyers; Kor H Hutting
Journal:  Ann Med Surg (Lond)       Date:  2021-05-27
  3 in total

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