Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/103784
Type: Artigo de periódico
Title: Molecular Screening Of Cftr Gene In Brazilian Men With Bilateral Agenesis Of The Vas Deferens
Author: Bertuzzo C.S.
Pinto Jr. W.
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 αF508/ 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. © British Fertility Society.
Editor: 
Rights: fechado
Identifier DOI: 10.1080/14647270500440598
Address: http://www.scopus.com/inward/record.url?eid=2-s2.0-33645633808&partnerID=40&md5=013f33ea3e641964465f231c52c261fc
Date Issue: 2006
Appears in Collections:Unicamp - Artigos e Outros Documentos

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