Fetal multicystic kidney disease: Outcome and follow up
Author(s) -
Sonja Pop-Trajković,
Aleksandar Ljubić,
Vesna Kopitović,
Vladimir Antić,
Jelena Milošević,
Milan Trenkić
Publication year - 2010
Publication title -
medicinski pregled
Language(s) - English
Resource type - Journals
eISSN - 1820-7383
pISSN - 0025-8105
DOI - 10.2298/mpns1004262p
Subject(s) - medicine , multicystic dysplastic kidney , pregnancy , kidney , autopsy , urinary system , kidney disease , fetus , prenatal diagnosis , renal agenesis , agenesis , surgery , obstetrics , genetics , biology
Congenital fetal anomalies are the great problem and one of the main causes of increased perinatal mortality and morbidity. The aim of this study is to determine the outcome of prenataly detected multicystic dysplastic kidney and to point to the necessity of postnatal diagnostic procedures.
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