Caroli's Syndrome with Autosomal Recessive Polycystic Kidney Disease in a Two Month Old Infant

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...

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Detalles Bibliográficos
Autores principales: Kim, Jeong Tae, Hur, Yoon Jeong, Park, Jee Min, Kim, Myung Joon, Park, Young Nyun, Lee, Jae Seung
Formato: Texto
Lenguaje:English
Publicado: Yonsei University College of Medicine 2006
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2687570/
https://www.ncbi.nlm.nih.gov/pubmed/16502495
http://dx.doi.org/10.3349/ymj.2006.47.1.131

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2687570/
https://www.ncbi.nlm.nih.gov/pubmed/16502495
http://dx.doi.org/10.3349/ymj.2006.47.1.131

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