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Thrombocytopenia and splenomegaly: an unusual presentation of congenital hepatic fibrosis
Congenital hepatic fibrosis (CHF) is a rare autosomal recessive disease that primarily affects the hepatobiliary and renal systems. It is characterized by hepatic fibrosis, portal hypertension, and renal cystic disease. Firm or hard hepatomegaly is present nearly in all patients, often with a promin...
| Autores principales: | , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2010
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2861643/ https://www.ncbi.nlm.nih.gov/pubmed/20384987 http://dx.doi.org/10.1186/1750-1172-5-4 |