A Rare Case of Autosomal Dominant Polycystic Kidney Disease Presenting in utero
Hema Dhumale, Yeshita Pujar, Bhavana Sherigar, Babasaheb Raosaheb Desai, Geeta Durdi, Anita Dalal
Citation Information :
Dhumale H, Pujar Y, Sherigar B, Desai BR, Durdi G, Dalal A. A Rare Case of Autosomal Dominant Polycystic Kidney Disease Presenting in utero. J South Asian Feder Obs Gynae 2011; 3 (1):44-45.
Copyright © 2011; Jaypee Brothers Medical Publishers (P) Ltd.
Echographic screening for autosomal dominant polycystic kidney disease from intrauterine life to adult life. Arch Ital Urol Nefrol Androl Jun 1991;63 (Suppl 2):89-92.
Diagnosis of fetal abnormalities: The 18-23 week scan. Diploma in fetal medicine series. The Parthenon Publishing Group, New York/London 1999;80-81.
A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16. Nature 1985;317:542-44.
Autosomal dominant polycystic kidney disease: Localization of the second gene to chromosome 4ql3-q23. Genomics 1993;18:467-72.
Prenatal diagnosis of adult polcystic kidney disease. Lancet 1983;2:337
Linkage, clinical features, and prognosis of autosomal dominant polycystic kidney disease types 1 and 2. J Am Soc Nephrol Oct 1996;7(10):2142-51.