Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF ) Freely available
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (9)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Wu, C.C.
Right arrow Articles by Chiang, H.S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Wu, C.C.
Right arrow Articles by Chiang, H.S.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Human Reproduction, Vol. 19, No. 2, 250-253, February 2004
© 2004 European Society of Human Reproduction and Embryology

Cystic fibrosis transmembrane conductance regulator gene screening and clinical correlation in Taiwanese males with congenital bilateral absence of the vas deferens

C.C. Wu1,2, H.M. Hsieh-Li1, Y.M. Lin3 and H.S. Chiang1,4,5

1 Graduate Institute of Medical Sciences, Taipei Medical University, Taipei, 2 Department of Urology, Taipei Medical University Hospital, Taipei, 3 Department of Urology, National Cheng Kung University Hospital, Tainan and 4 College of Medicine, Fu Jen Catholic University, Taipei, Taiwan

5 To whom correspondence should be addressed at: College of Medicine, Fu Jen Catholic University, 510 Chung Cheng Road, Hsinchuang, Taipei Hsien 24205, Taiwan. e-mail: hansun{at}tmu.edu.tw

BACKGROUND: In Taiwan, an area with a very low incidence of cystic fibrosis (CF), we first screened for the most common mutations of the cystic fibrosis transmembrane conductance regulator (CFTR) gene and looked for clinical correlations in 27 patients with clinically diagnosed congenital bilateral absence of the vas deferens (CBAVD). METHODS AND RESULTS: The clinical results showed that none of the 27 patients had CF symptoms. We did not detect any definite renal anomaly ultrasonographically. Mutation analysis was carried out on these 27 cases and 46 normal fertile males as controls. No mutations of {Delta}F508 or R117H were identified in any of the samples analysed. In the screening of IVS8-poly T, five of the 27 CBAVD patients showed the homozygous genotype for 5T/5T, 14 showed the heterozygous genotype for 5T/7T and eight showed the homozygous genotype for 7T/7T. The frequency of 5T alleles was 44.4%, which was significantly higher than in the 46 normal fertile males, for which there was a 5T frequency of 5.4%. CONCLUSIONS: The absence of major mutations of CFTR genes could be related to the much lower CF incidence in Taiwan. Further investigations into differences in the mutation spectrum of other CFTR genes are needed for a better understanding of the development of Taiwanese-Oriental CBAVD.

Key words: congenital bilateral absence of the vas deferens/cystic fibrosis/cystic fibrosis transmembrane conductance regulator/gene screening/male infertility


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
J AndrolHome page
R. Radpour, H. Gourabi, M. A. S. Gilani, and A. V. Dizaj
Molecular Study of (TG)m(T)n Polymorphisms in Iranian Males With Congenital Bilateral Absence of the Vas Deferens
J Androl, July 1, 2007; 28(4): 541 - 547.
[Abstract] [Full Text] [PDF]


Home page
Mol Hum ReprodHome page
R. Radpour, M. A. S. Gilani, H. Gourabi, A. V. Dizaj, and S. Mollamohamadi
Molecular analysis of the IVS8-T splice variant 5T and M470V exon 10 missense polymorphism in Iranian males with congenital bilateral absence of the vas deferens
Mol. Hum. Reprod., July 1, 2006; 12(7): 469 - 473.
[Abstract] [Full Text] [PDF]


Home page
Hum ReprodHome page
C.-C. Wu, O. M. Alper, J.-F. Lu, S.-P. Wang, L. Guo, H.-S. Chiang, and L.-J. C. Wong
Mutation spectrum of the CFTR gene in Taiwanese patients with congenital bilateral absence of the vas deferens
Hum. Reprod., September 1, 2005; 20(9): 2470 - 2475.
[Abstract] [Full Text] [PDF]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.