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[Unilateral partial deferential agenesia and CFTR gene composite heterozygoty (deltaF508/V938G)]. / Agénésie déférentielle partielle unilatérale et hétérozygotie composite du gène CFTR (DeltaF508/V938G).
Robin, G; Lefèbvre-Khalil, V; Dumur, V; Lemaître, L; Mitchell, V; Rigot, J-M; Marcelli, F.
  • Robin G; Service d'Andrologie, Hôpital Calmette, CHRU de Lille, Lille cedex, France. geoffroy.robin@laposte.net <geoffroy.robin@laposte.net>
Gynecol Obstet Fertil ; 35(6): 561-4, 2007 Jun.
Article en Fr | MEDLINE | ID: mdl-17507277
ABSTRACT
This is a case report of a thirty-year-old-man consulting for a primary infertility that was diagnosed four years ago. Andrologic exam was normal. Two spermograms found normal spermatic parameters. An uro-genital echography with a RMI showed that a unilateral agenesia of the left vas deferens in the pelvic portion. Then, a composite heterozygoty of the CFTR gene (DeltaF508/V938G) was found. This is the first time that the association of these two mutations has been described. This case also makes it possible to wonder about the need for realizing, or not, a systematic basis imagery (ultrasound examination in first), in the event of infertility of the couple. In this context, the discovery of an echographic anomaly made it possible to identify CFTR mutations, whose physiopathological implication in the infertility can be discussed (CFTR related disorders)...
Asunto(s)
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Banco de datos: MEDLINE Asunto principal: Conducto Deferente / Regulador de Conductancia de Transmembrana de Fibrosis Quística / Infertilidad Masculina / Mutación Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Adult / Humans / Male Idioma: Fr Año: 2007 Tipo del documento: Article
Search on Google
Banco de datos: MEDLINE Asunto principal: Conducto Deferente / Regulador de Conductancia de Transmembrana de Fibrosis Quística / Infertilidad Masculina / Mutación Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Adult / Humans / Male Idioma: Fr Año: 2007 Tipo del documento: Article