elevations of transaminases to life-threatening fulminant liver disease. […] Hepatolenticular degeneration was first discovered while studying the brain damages associated with liver diseases. […] In patients with a fulminant liver disease, liver transplantation is recommended and good long-term results have been observed.
Seminar in Liver Disease. 2001;21(4):535–544. […] Seminars in Liver Disease. 2001;21(4):551–562. […] Liver diseases related to MDR3 (ABCB4) gene deficiency.
Bile acid synthetic defects and liver disease: a comprehensive review. […] Liver disease caused by failure to racemize trihydroxycholestanoic acid: gene mutation and effect of bile acid therapy. […] Setchell KD, Heubi JE, Bove KE, et al., Jr Liver disease caused by failure to racemize trihydroxycholestanoic acid: gene mutation and effect of bile acid therapy.
Lung and liver disease are the preliminary features of AATD. […] Alcohol should be avoided as it would further aggravate the condition in individuals suffering from liver disease as a secondary complication of AAT.
Alcoholic liver disease. […] Alcoholic liver disease. […] The epidemiology of alcoholic liver disease.
Alcoholic liver disease. […] Alcoholic liver disease and hepatitis C: a frequently underestimated combination. […] Individuals who consume moderate to excess alcohol fall easy prey to this liver disease.
Mortality attributable to cholestatic liver disease in the United States. […] The enzyme levels would give an indication of liver disease and extent of damage to bile ducts. […] Definition Primary biliary cirrhosis abbreviated as PBC is a chronic liver disease that gradually damages the bile ducts.
It is less common than alcoholic liver disease, but is one of the leading cause for liver transplantation in the US. […] Primary sclerosing cholangitis (PSC) is a chronic, progressive, cholestatic liver disease characterized by fibrosis and inflammation of intra- and extrahepatic biliary ducts […] Primary sclerosing cholangitis (PSC) is a chronic liver disease in which the bile ducts progressively undergo scarring and inflammation, narrowing the lumen.
Progressive neuronal degeneration of childhood with liver disease (Alpers-Huttenlocher syndrome): a personal review. […] Liver involvement progresses to end stage liver disease characterized by hypoalbuminemia, coagulopathy and hyperammonemia. […] Alpers syndrome is a rare neurodevelopmental mitochondrial DNA depletion syndrome which is characterized by seizures, progressive encephalopathy and liver disease.
A few people may have a more severe form of liver disease known as (fulminant hepatic failure) and may die as a result.