Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/196702
Type: Artigo de periódico
Title: Molecular Screening Of Cftr Gene In Brazilian Men With Bilateral Agenesis Of The Vas Deferens.
Author: Bertuzzo, Carmen Sílvia
Pinto, Walter
Abstract: Infertility is a common symptom of cystic fibrosis, especially in men (95% become sterile). It is caused by blockage of the vas deferens and the epididymis, which result in degeneration of the tubules. The purpose of this study was to verify the frequency of CFTR gene mutation in patients with bilateral agenesis of the vas deferens using SSCP and sequencing. The study population consisted of 40 white individuals with agenesis of the vas deferens as well as their 12 siblings without agenesis of the vas deferens. CTFR gene mutation was found in 22 of the 40 patients (55%) and it was possible to detect both mutating alleles in these 22 patients. The most frequent genotype found was ?F508/IVS8-5T. There was no genotype concordance in siblings. Our results show the importance of the investigation of CFTR mutation in patients with vas deferens agenesis.
Subject: Adult
Brazil
Cystic Fibrosis
Cystic Fibrosis Transmembrane Conductance Regulator
Genetic Testing
Genotype
Humans
Infertility, Male
Male
Mutation
Vas Deferens
Rights: fechado
Identifier DOI: 10.1080/14647270500440598
Address: http://www.ncbi.nlm.nih.gov/pubmed/16581722
Date Issue: 2006
Appears in Collections:Artigos e Materiais de Revistas Científicas - Unicamp

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.