Literature DB >> 12475673

Clinical and genetic features of patients with congenital unilateral absence of the vas deferens.

Peter N Kolettis1, Jay I Sandlow.   

Abstract

OBJECTIVES: To review the clinical and genetic findings in men with congenital unilateral absence of the vas deferens (CUAVD). CUAVD is important because of its association with renal anomalies and cystic fibrosis transmembrane conductance regulator gene mutations.
METHODS: A retrospective review of two urologic practices, both with subspecialty interest in male infertility, was performed. Renal imaging and cystic fibrosis (CF) testing were recommended to all men found to have CUAVD.
RESULTS: Fifteen men with CUAVD were identified. Only the 12 men with sufficient clinical data were selected for this study. Three patients had CF mutations, and all had obstruction of the contralateral vas deferens in either the pelvis or retroperitoneum. One patient had obstruction of the contralateral pelvic vas deferens and was negative for all CF mutations tested. Four patients (33%) had renal agenesis. Three patients had ipsilateral renal agenesis, and one had contralateral renal agenesis. No patient with CF mutations had renal agenesis. One had polycystic kidney disease, which was considered an incidental finding.
CONCLUSIONS: Patients with CUAVD may have CF mutations and renal agenesis. Renal ultrasonography and CF testing are therefore recommended for these patients. Patients of reproductive age found to have CUAVD should be counseled about the potential risk of transmission of renal anomalies and CF mutations.

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Year:  2002        PMID: 12475673     DOI: 10.1016/s0090-4295(02)01973-8

Source DB:  PubMed          Journal:  Urology        ISSN: 0090-4295            Impact factor:   2.649


  9 in total

1.  Steps in the investigation and management of low semen volume in the infertile man.

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2.  CFTR mutations causing congenital unilateral absence of the vas deferens (CUAVD) and congenital absence of the uterus (CAU) in a consanguineous family.

Authors:  Mahdieh Daliri Ghouchanatigh; Ranjha Khan; Majid Mojarrad; Uzma Hameed; Muhammad Zubair; Ahmed Waqas; Mohsen Jalali; Mahmoudreza Kalantari; Ali Shamsa; Huan Zhang; Qing-Hua Shi
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3.  Genetic etiology of renal agenesis: fine mapping of Renag1 and identification of Kit as the candidate functional gene.

Authors:  Nyssa Becker Samanas; Tessa W Commers; Kirsten L Dennison; Quincy Eckert Harenda; Scott G Kurz; Cynthia M Lachel; Kristen Leland Wavrin; Michael Bowler; Isaac J Nijman; Victor Guryev; Edwin Cuppen; Norbert Hubner; Ruth Sullivan; Chad M Vezina; James D Shull
Journal:  PLoS One       Date:  2015-02-18       Impact factor: 3.240

4.  Congenital absence of vas deferens and ectopic kidney.

Authors:  Alobaidi Salwan; Alhmooze Abdelrahman
Journal:  Int J Surg Case Rep       Date:  2017-03-18

5.  CFTR variants and renal abnormalities in males with congenital unilateral absence of the vas deferens (CUAVD): a systematic review and meta-analysis of observational studies.

Authors:  Hongcai Cai; Xingrong Qing; Jean Damascene Niringiyumukiza; Xuxin Zhan; Dunsheng Mo; Yuanzhong Zhou; Xuejun Shang
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Review 6.  Genetic testing for men with infertility: techniques and indications.

Authors:  Daniel L Pelzman; Kathleen Hwang
Journal:  Transl Androl Urol       Date:  2021-03

Review 7.  A comprehensive review of genetics and genetic testing in azoospermia.

Authors:  Alaa J Hamada; Sandro C Esteves; Ashok Agarwal
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8.  A case of congenital unilateral absence of the vas deferens.

Authors:  Bi Mo; Vishnu Garla; Lawrence M Wyner
Journal:  Int Med Case Rep J       Date:  2013-04-15

9.  Unilateral absence of vas deferens: prevalence among 23.013 men seeking vasectomy.

Authors:  Sarah Miller; Sophie Couture; Gareth James; Simon Plourde; Jacky Rioux; Michel Labrecque
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  9 in total

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