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[Prenatal exclusion of von Hippel-Lindau syndrome in a Mexican family carrying a novel VHL gene mutation].

Ginecologia y obstetricia de Mexico - 1 Mar 2014

Chacón-Camacho Oscar Francisco, Benitez-Granados Jesús, Zenteno Juan Carlos

Abstract excerpt

BACKGROUND: von Hippel-Lindau (VHL) disease is an autosomal dominant and familial multisystemic syndrome that is caused by the inactivation of the VHL gene and it is characterized by diverse types of high vasculated tumours of benign and malign nature. In this work we describe the clinical characteristics and the prenatal diagnosis of a woman with VHL. OBJECTIVE: Describe the first exclusion prenatal case by DNA...

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PMID: 24779271

Genes

VHL

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[Prenatal exclusion of von Hippel-Lindau syndrome in a Mexican family carrying a novel VHL gene mutation].PMID 24779271Read ↗

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