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Autosomal recessive polycystic kidney disease (ARPKD)--a report of two cases
R V Ramteke1, A S Vyas, K S Bhople
1Department of Pathology, Government Medical College & Hospital, Aurangabad.
Indian Journal of Pathology & Microbiology
|October 1, 1995
Abstract:
Autosomal Recessive Polycystic Kidney (ARPKD) is a very rare entity (1 in 15,000 live births) and mostly not compatible with life. Early diagnosis and genetic councelling may help prevent such births. Two interested cases are presented.