Autosomal recessive polycystic kidney disease and congenital hepatic fibrosis (ARPKD/CHF)

ARPKD/CHF is an inherited disease characterized by non-obstructive fusiform dilatation of the renal collecting ducts leading to enlarged spongiform kidneys and ductal plate malformation of the liver resulting in congenital hepatic fibrosis. ARPKD/CHF has a broad spectrum of clinical presentations in...

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Autores principales: Turkbey, Baris, Ocak, Iclal, Daryanani, Kailash, Font-Montgomery, Esperanza, Lukose, Linda, Bryant, Joy, Tuchman, Maya, Mohan, Parvathi, Heller, Theo, Gahl, William A., Choyke, Peter L., Gunay-Aygun, Meral
Formato: Artigo
Lenguaje:Inglês
Publicado: 2008
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Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC2918426/
https://ncbi.nlm.nih.gov/pubmed/19089418
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00247-008-1064-x
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