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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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Detalhes bibliográficos
Main Authors: Kim, Jeong Tae, Hur, Yoon Jeong, Park, Jee Min, Kim, Myung Joon, Park, Young Nyun, Lee, Jae Seung
Formato: Artigo
Idioma:Inglês
Publicado em: Yonsei University College of Medicine 2006
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2687570/
https://ncbi.nlm.nih.gov/pubmed/16502495
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3349/ymj.2006.47.1.131
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