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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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Main Authors: | , , , , , |
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Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
Yonsei University College of Medicine
2006
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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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