Hepatic arteriovenous malformation with hyperammonemia in rendu-osler-weber syndrome

Journal of Gastrointestinal and Liver Diseases

Volumn 20, Issue 3, 2011, Pages 330-331

  Taguchi, Takafumi ^a   Iwamura, Shinichi ^b   Mizobuchi, Miki ^b   Terada, Yoshio ^a  

^a KOCHI MEDICAL SCHOOL   (Japan)

^b KOCHI RED CROSS HOSPITAL   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ALANINE AMINOTRANSFERASE; ALKALINE PHOSPHATASE; AMMONIA; ASPARTATE AMINOTRANSFERASE; GAMMA GLUTAMYLTRANSFERASE; HEMOGLOBIN;

ADULT; ALANINE AMINOTRANSFERASE BLOOD LEVEL; ALKALINE PHOSPHATASE BLOOD LEVEL; AMMONIA BLOOD LEVEL; ANEMIA; ARTERIOVENOUS MALFORMATION; ASPARTATE AMINOTRANSFERASE BLOOD LEVEL; CASE REPORT; COMPUTER ASSISTED TOMOGRAPHY; EPISTAXIS; FAMILY HISTORY; FEMALE; GAMMA GLUTAMYL TRANSFERASE BLOOD LEVEL; HEMOGLOBIN BLOOD LEVEL; HEPATIC ARTERIOVENOUS MALFORMATION; HUMAN; HYPERAMMONEMIA; LASER SURGERY; LETTER; LIVER ARTERIOGRAPHY; LIVER DISEASE; RENDU OSLER WEBER DISEASE;

ARTERIOVENOUS MALFORMATIONS; FEMALE; HUMANS; HYPERAMMONEMIA; LIVER; MIDDLE AGED; TELANGIECTASIA, HEREDITARY HEMORRHAGIC;

EID: 80053541377     PISSN: 18418724     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (5)

1. Shovlin CL, Guttmacher AE, Buscarini E, et al. Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome). Am J Med Genet 2000;91:66-67.
2. Plauchu H, Dupuis-Girod S. Hereditary hemorrhagic telangiectasia. Rev Prat 2009;59:899-903.
3. Sharathkumar AA, Shapiro A. Hereditary haemorrhagic telangiectasia. Haemophilia 2008;14:1269-1280.
4. Sabba C, Pompili M. Review article: the hepatic manifestations of hereditary haemorrhagic telangiectasia. Aliment Pharmacol Ther 2008;28:523-533.
5. Alexander BG, Khoo EW, Arstall MA, Roberts-Thomson IC. Education and imaging. Hepatobiliary and pancreatic: hepatic arteriovenous malformations in hereditary hemorrhagic telangiectasia. J Gastroenterol Hepatol 2007;22:1549.