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Predominant extrahepatic biliary disease in autosomal recessive polycystic kidney disease: A new association

✍ Scribed by Beatrice Goilav; Karen I. Norton; Lisa M. Satlin; Lisa Guay-Woodford; Frank Chen; Margret S. Magid; Sukru Emre; Benjamin L. Shneider

Book ID
110896020
Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
306 KB
Volume
10
Category
Article
ISSN
1397-3142

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## Communicated by Jurgen Horst Autosomal recessive polycystic kidney disease (ARPKD) is an important cause of childhood renal-and liverrelated morbidity and mortality. The clinical spectrum is widely variable. About 30 to 50% of affected individuals die in the neonatal period, while others survive