Cirrhosis causes
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] ; Associate Editor(s)-in-Chief: Aditya Govindavarjhulla, M.B.B.S. [2]
Overview
Causes
Common Causes
Cirrhosis has many possible causes; sometimes more than one cause is present in the same patient. In the Western World, chronic alcoholism and hepatitis C are the most common causes.
- Alcoholic liver disease
- Chronic hepatitis C
- Chronic hepatitis B
- Non-alcoholic steatohepatitis (NASH)
- Primary biliary cirrhosis
- Primary sclerosing cholangitis
- Autoimmune hepatitis
- Hereditary hemochromatosis
- Wilson's disease
- Alpha 1-antitrypsin deficiency
- Cardiac cirrhosis
- Galactosemia
- Glycogen storage disease type IV
- Cystic fibrosis
- Drugs or toxins
- Certain parasitic infections (such as schistosomiasis)
Causes by Organ System
Causes in Alphabetical Order [1] [2]
- Abetalipoproteinemia
- Acetaminophen overdose
- Addison-Gull syndrome
- Aflatoxin
- Alagille syndrome
- Alcoholic liver disease
- Alpers disease
- Alpha 1-antitrypsin deficiency
- Alström syndrome
- Amiodarone
- Autoimmune cholangiopathy
- Autoimmune hepatitis
- Bearn-Kunkel syndrome [3]
- Berardinelli lipodystrophy syndrome
- Bile duct stricture
- Biliary atresia
- Budd-Chiari Syndrome
- Carbohydrate deficient glycoprotein syndrome type 1a
- Cardiac cirrhosis
- Caroli disease
- Cerebrohepatorenal syndrome
- Ceroid storage disease
- Cholestasis-oedema syndrome, Norwegian type
- Cholesterol ester storage disease
- Congenital hepatic fibrosis
- Constrictive pericarditis
- Cor Pulmonale
- Cruveilhier-Baumgarten syndrome
- Cystic fibrosis
- Erythropoietic protoporphyria
- Ethanol
- Fanconi disease [4]
- Fasciola hepatica
- Fructose-1-phosphate aldolase deficiency [5]
- Galactosemia
- Glycogen storage disease type IV
- Graft versus host disease
- Granulomatous cirrhosis
- Haemosiderosis
- Hemochromatosis
- Hepatic vein thrombosis
- Hepatitis B
- Hepatitis C
- Hereditary fructose intolerance
- Hypervitaminosis A
- Indian familial childhood cirrhosis
- Isoniazid
- Keratitis-ichthyosis-deafness syndrome, autosomal recessive
- Methotrexate
- Methyldopa
- Non-alcoholic steatohepatitis
- Parenteral nutrition
- Polycystic kidney disease, autosomal recessive
- Porphyria cutanea tarda type 2 (familial)
- Primary biliary cirrhosis
- Primary sclerosing cholangitis
- Reynolds syndrome [6]
- Right sided cardiac failure
- Sarcoidosis
- Schistosomiasis
- Sickle Cell Disease
- Steatohepatitis
- Thalassemia
- Tricho-hepato-enteric syndrome [7]
- Tricuspid insufficiency
- Tyrosinaemia type 1
- Visceral leishmaniasis
- Wilson disease
References
- ↑ Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:77 ISBN 1591032016
- ↑ Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:68 ISBN 140510368X
- ↑ http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1813854/#reference-sec
- ↑ http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2165837/
- ↑ http://ghr.nlm.nih.gov/condition/hereditary-fructose-intolerance
- ↑ http://rarediseases.info.nih.gov/GARD/Condition/4697/Reynolds_syndrome.aspx
- ↑ http://www.checkorphan.org/disease/tricho-hepato-enteric-syndrome