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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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| Pubblicato in: | Cureus |
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| Autori principali: | , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Cureus
2019
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6827873/ https://ncbi.nlm.nih.gov/pubmed/31728235 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7759/cureus.5788 |
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