Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

[Role of deep seminal tract imaging in the diagnosis of unilateral agenesis of the vas deferens. Case report of a patient with CFTR gene mutation].

Progres en urologie : journal de l'Association francaise d'urologie et de la Societe francaise d'urologie - 1 Nov 2006

Marcelli François, Robin Geoffroy, Mitchell Valérie, Dumur Viviane, Puech Philippe, Lemaitre Laurent, Rigot Jean-Marc

Abstract excerpt

The authors report the cases of a 35-year-old man with a 4-year history of primary infertility with normal clinical examination and semen parameters. Deep genital tract imaging demonstrated isolated unilateral agenesis of the pelvic portion of the left vas deferens associated with abnormalities of the homolateral seminal vesicle. Molecular analysis of the CFTR gene demonstrated composite heterozygosity with the...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Cystic Fibrosis Transmembrane Conductance Regulator
Share to CFTR gene

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Infertility, Male

Share to Magnetic Resonance Imaging

Share to Mutation

Share to Vas Deferens

Source

Identifiers

PMID: 17175965

Genes

CFTR

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Role of deep seminal tract imaging in the diagnosis of unilateral agenesis of the vas deferens. Case report of a patient with CFTR gene mutation].PMID 17175965Read ↗

A patient with 47, XYY mosaic karyotype and congenital absence of bilateral vas deferens: a case report and literature review.Semantic proximity Read ↗

Mutations of the cystic fibrosis transmembrane conductance regulator gene in males with congenital bilateral absence of the vas deferens: Reproductive implications and genetic counseling (Review).Semantic proximity Read ↗

[Agenesis of the vas deferens in male infertility. A tentative classification based on 39 cases].Semantic proximity Read ↗

Congenital bilateral absence of the vas deferens as an atypical form of cystic fibrosis: reproductive implications and genetic counselingSemantic proximity Read ↗

Molecular screening of CFTR gene in Brazilian men with bilateral agenesis of the vas deferens.Semantic proximity Read ↗

Genetic investigations of CFTR mutations in congenital absence of vas deferens, uterus, and vagina as a cause of infertility.Semantic proximity Read ↗

[Gene mutations in congenital bilateral absence of the vas deferens: An update].Semantic proximity Read ↗

Correlation between CFTR gene mutations in Iranian men with congenital absence of the vas deferens and anatomical genital phenotype.Semantic proximity Read ↗

[Agenesis of vas deferens and cystic fibrosis].Semantic proximity Read ↗

[Unilateral partial deferential agenesia and CFTR gene composite heterozygoty (deltaF508/V938G)].Semantic proximity Read ↗

Cystic fibrosis transmembrane regulator mutation and congenital bilateral absence of the vas deferens: a bad combination for successful intracytoplasmic sperm injection outcomes.Semantic proximity Read ↗

[Genetically determined male infertility caused by the CFTR gene mutations].Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.