Familial cirrhosis
From Wikipedia, the free encyclopedia
Medical condition
Familial 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.[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.
It is associated with KRT8 and KRT18.[1]
References[]
External links[]
Diseases of the digestive system | |||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|
Upper GI tract |
| ||||||||||
Lower GI tract Enteropathy |
| ||||||||||
GI bleeding |
| ||||||||||
Accessory |
| ||||||||||
Other |
|
![]() | This article about a disease, disorder, or medical condition is a stub. You can help Wikipedia by . |
- v
- t
Retrieved from ""
Categories:
- Congenital disorders of digestive system
- Cytoskeletal defects
- Disease stubs
Hidden categories:
- Articles with short description
- Short description is different from Wikidata
- All articles with unsourced statements
- Articles with unsourced statements from September 2021
- All stub articles