Familial cirrhosis

From Infogalactic: the planetary knowledge core
Jump to: navigation, search
Familial cirrhosis
Classification and external resources
Specialty Lua error in Module:Wikidata at line 446: attempt to index field 'wikibase' (a nil value).
ICD-9-CM 571.5
OMIM 215600
Patient UK Familial cirrhosis
[[[d:Lua error in Module:Wikidata at line 863: attempt to index field 'wikibase' (a nil value).|edit on Wikidata]]]

Familial cirrhosis is a form of cirrhosis that is a keratin disease. This particular type of cirrhosis is inherited and the liver scarring is not caused by any obvious disease process. 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.[1]

References

http://www.rightdiagnosis.com/medical/familial_cirrhosis.htm


<templatestyles src="Asbox/styles.css"></templatestyles>