Caroli's Syndrome with Autosomal Recessive Polycystic Kidney Disease in a Two Month Old Infant
Yonsei Medical Journal
; : 131-134, 2006.
Article
in En
| WPRIM
| ID: wpr-116909
Responsible library:
WPRO
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.
Key words
Full text:
1
Index:
WPRIM
Main subject:
Polycystic Kidney, Autosomal Recessive
/
Caroli Disease
/
Hepatic Duct, Common
/
Kidney
Limits:
Humans
/
Infant
/
Male
Language:
En
Journal:
Yonsei Medical Journal
Year:
2006
Type:
Article