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Congenital hepatic fibrosis and coexistent retinal macular degeneration: A case report
RATIONALE: Congenital hepatic fibrosis (CHF) is an autosomal recessive disease characterized by periportal fibrosis, portal hypertension, and renal cystic disease. Essentially, CHF is a variant of fibrocystic disorder in which liver and kidney are commonly affected. Other frequently associated condi...
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| Publicado no: | Medicine (Baltimore) |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Wolters Kluwer Health
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6736369/ https://ncbi.nlm.nih.gov/pubmed/31464924 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000016909 |
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