A Case of Congenital Hepatic Fibrosis

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Congenital hepatic fibrosis in an aborted calf

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Congenital Hepatic Fibrosis: An Uncommon Cause of Chronic Renal Failure

Congenital Hepatic Fibrosis (CHF) is a rare disease that affects both the liver and kidneys.  Congenital hepatic fibrosis (CHF) is an autosomal recessive inherited malformation defined pathologically by a variable degree of periportal fibrosis and irregularly shaped proliferating bile ducts. Affected individuals also have impaired renal function, usually caused, in children and teenagers, by an...

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Congenital hepatic fibrosis.

Congenital Hepatic fibrosis is an uncommon disease, which is autosomal recessive. Two forms of the disease are distinguished: a rare one becoming manifest in the neonatal period with signs of progressive renal failure secondary to polycystic kidneys, in such cases the liver fibrosis is usually asymptomatic, and the diagnosis is therefore often first established post mortem. In the other more us...

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Congenital hepatic fibrosis

CONGENITAL hepatic fibrosis is an uncommon cause of portal hypertension and usually presents as alimentary bleeding in childhood or adolescence. The occurrence in more than one member of a family has been described (Kerr et al., 1961; Campbell et al., 1958). This report concerns four members of one family who have presented with clinical features attributable to congenital hepatic fibrosis. Pat...

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ژورنال

عنوان ژورنال: The Journal of Tepecik Education and Research Hospital

سال: 1995

ISSN: 1305-7073

DOI: 10.5222/terh.1995.08835