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P09.10: Early diagnosis of autosomal recessive polycystic kidney disease (ARPKD)—a case report

✍ Scribed by A. Ayed; P. Sinha; N. Roberts; M. Mishra

Book ID
112231922
Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
49 KB
Volume
38
Category
Article
ISSN
0960-7692

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## Background: Autosomal-recessive polycystic kidney disease (arpkd) is an important neonatal nephropathy characterized by fusiform dilation of collecting ducts, congenital hepatic fibrosis, and in some cases caroli's disease. the arpkd gene, pkhd1, has recently been identified. herein we describe