Familial cirrhosis

Familial cirrhosis
Liver Cirrhosis.
Specialty	Hepatology

Familial cirrhosis is a form of liver disease that is inherited and the liver scarring is not caused by any obvious disease process. This type of cirrhosis is a keratin disease. Damage progresses until function becomes impaired.

Current cirrhosis treatment is aimed at managing complications as well as chronic poor health related to liver damage. Treatments include abstinence from alcohol, nutritional supplement, identification of any identifiable disease process, management of portal hypertension, and liver transplantation.

It is associated with KRT8 and KRT18.

See also

• Keratin disease
• Cirrhosis

Further reading

• MacSween, R. N. M.; Fell, G. S. (1974). "Familial Cirrhosis". Scottish Medical Journal. 19 (1). SAGE Publications: 25–30. doi:10.1177/003693307401900107. ISSN 0036-9330. PMID 4820008. S2CID 40700728.
• MADDREY, WILLIS C. (October 1, 1964). "Familial Cirrhosis". Annals of Internal Medicine. 61 (4). American College of Physicians: 667–679. doi:10.7326/0003-4819-61-4-667. ISSN 0003-4819. PMID 14217129.
• Scorza, Manuela; Elce, Ausilia; Zarrilli, Federica; Liguori, Renato; Amato, Felice; Castaldo, Giuseppe (2014). "Genetic Diseases That Predispose to Early Liver Cirrhosis". International Journal of Hepatology. 2014. Hindawi Limited: 1–11. doi:10.1155/2014/713754. ISSN 2090-3448.