PMID: 16502495Feb 28, 2006Paper

Caroli's syndrome with autosomal recessive polycystic kidney disease in a two month old infant

Yonsei Medical Journal
Jeong Tae KimJae Seung Lee

Abstract

Caroli's syndrome is a rare congenital disorder that involves intrahepatic bile duct ectasia and congenital hepatic fibrosis, frequently seen with concomitant autosomal recessive polycystic kidney disease (ARPKD). Literature on infants with ARPKD is rare. Here, we present a case of a two month old boy who was diagnosed with Caroli's syndrome and ARPKD.

References

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Citations

Sep 25, 2012·World Journal of Gastroenterology : WJG·Beata Jabłońska
May 24, 2008·International Journal of Surgical Pathology·Shramana MandalA K Mandal
Dec 29, 2020·Clinical Case Reports·Akash RautBikal Ghimire

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