Familial cirrhosis

In today's world, Familial cirrhosis is a topic that arouses great interest and debate among society. Whether due to its historical relevance, its impact on popular culture, or its influence in the scientific field, Familial cirrhosis has captured the attention of thousands of people around the world. As we further explore this fascinating topic, it is important to open our eyes to its many facets and understand how it has shaped and will continue to shape our present and future. In this article, we will delve into the importance and meaning of Familial cirrhosis, examine its impact on different aspects of society, and explore the various perspectives that exist around this topic.
Familial cirrhosis
Liver Cirrhosis.
SpecialtyHepatology

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.[citation needed]

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.[citation needed]

It is associated with KRT8 and KRT18.[1]

See also

References

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.