[Autosomal dominant polycystic kidney disease in a large family].
The diagnosis of autosomal dominant polycystic kidney disease (ADPKD) was established in persons (6 adult and 8 children) among 34 members of a three generations family. The presence of coexisting cysts in liver was ascertained in 3 women, and the presence of ovarian cysts was discovered in a 14 years old girl. Arterial hypertension was observed in 2 men and 2 women. The symptoms of initiating renal failure were found in 1 patient. The clinical observation of the most numerous among described in accessible literature family will be continued.
Adolescent↗