Caroli's Syndrome with Autosomal Recessive Polycystic Kidney Disease in a Two Month Old Infant
Yonsei Medical Journal
; : 131-134, 2006.
Article
en En
| WPRIM
| ID: wpr-116909
Biblioteca responsable:
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.
Palabras clave
Texto completo:
1
Índice:
WPRIM
Asunto principal:
Riñón Poliquístico Autosómico Recesivo
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Enfermedad de Caroli
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Conducto Hepático Común
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Riñón
Límite:
Humans
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Infant
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Male
Idioma:
En
Revista:
Yonsei Medical Journal
Año:
2006
Tipo del documento:
Article