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

Author:

de Souza D. A. S.12,Faucz F. R.13,Pereira-Ferrari L.4,Sotomaior V. S.1,Raskin S.1ORCID

Affiliation:

1. Group for Advanced Molecular Investigation (NIMA); School of Health and Biosciences; Pontifícia Universidade Católica do Paraná (PUCPR); Curitiba PR Brazil

2. Functional Genomics Laboratory; Carlos Chagas Institute; Oswaldo Cruz Foundation; Curitiba PR Brazil

3. Section on Endocrinology & Genetics; Program on Developmental Endocrinology & Genetics; Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD); NIH; Bethesda MD USA

4. Department of Biomedicine; UniBrasil; Curitiba PR Brazil

Funder

Eunice Kennedy Shriver National Institute of Child Health and Human Development

National Institutes of Health

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Publisher

Wiley

Subject

Urology,Endocrinology,Reproductive Medicine,Endocrinology, Diabetes and Metabolism

Reference93 articles.

1. Link between CFTR mutations and ABPA: a systematic review and meta-analyses;Agarwal;Mycoses,2012

2. Pregnancy outcomes after assisted reproductive technology;Allen;J Obstet Gynaecol Can,2006

3. Congenital bilateral absence of the vas deferens. A primarily genital form of cystic fibrosis;Anguiano;JAMA,1992

4. Congenital bilateral absence of vas deferens with a new missense mutation (P499A) in the CFTR gene;Arduino;Clin Genet,1998

5. Genetic, andrological and clinical characteristics of patients with congenital bilateral absence of the vas deferens;Attardo;Int J Urol,2001

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