An Unusual Case of Congenital Hepatic Fibrosis with Retinitis Pigmentosa

Congenital hepatic fibrosis (CHF) is a rare hereditary autosomal recessive disorder due to periportal fibrosis and ductal plate malformation. It is just one of many different malformations collectively named oculo-encephalo-hepato-renal syndrome. The major presenting feature is upper gastrointestina...

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Detalles Bibliográficos
Autores principales: Butt, Nazish, Akbar, Ali, Fahad, Anoshia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2019
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6827873/
https://www.ncbi.nlm.nih.gov/pubmed/31728235
http://dx.doi.org/10.7759/cureus.5788

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6827873/
https://www.ncbi.nlm.nih.gov/pubmed/31728235
http://dx.doi.org/10.7759/cureus.5788

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