Diagnosis and Management of Hepatobiliary Complications in Autosomal Recessive Polycystic Kidney Disease

Autosomal recessive polycystic kidney disease (ARPKD) is a congenital hepatorenal fibrocystic disease. The hepatic manifestations of ARPKD can range from asymptomatic to portal hypertension and massively dilated biliary system that results in liver transplantation. Hepatic complications of ARPKD typ...

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Detalles Bibliográficos
Autores principales: Wehrman, Andrew, Kriegermeier, Alyssa, Wen, Jessica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5446979/
https://www.ncbi.nlm.nih.gov/pubmed/28611971
http://dx.doi.org/10.3389/fped.2017.00124

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5446979/
https://www.ncbi.nlm.nih.gov/pubmed/28611971
http://dx.doi.org/10.3389/fped.2017.00124

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