PMID: 9417467Jan 1, 1997Paper

Autosomal dominant polycystic kidney. Apropos of 2 cases. Review of the literature

Journal de gynécologie, obstétrique et biologie de la reproduction
V TsatsarisS Uzan

Abstract

Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary disease. Genetic molecular methods can make the diagnosis of at least three different types of ADPKD. ADPKD concerns young people and complications such as hypertension and decreased renal function occur more frequently if onset is early, if it is a type 1, and if the patient is a woman. The pregnant woman with autosomal dominant cystic disease is at particular high risk of obstetrical complications. Prenatal diagnosis is possible.

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