HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Diffuse fatty liver in familial heterozygous hypobetalipoproteinemia.

Abstract
A 34-year-old man had asymptomatic hepatomegaly, slightly increased serum alanine aminotransferase and gamma-glutamyl transpeptidase levels, and a sonographic pattern suggesting diffuse hepatic steatosis. Liver biopsy revealed fatty change in 25% to 50% of hepatocytes. The patient also had low serum levels of cholesterol and triglycerides and met clinical, biochemical, and familial diagnostic criteria of heterozygous hypobetalipoproteinemia. We could not relate his hepatic steatosis to any already known cause of fatty liver and could only attribute it to heterozygous hypobetalipoproteinemia. Familial heterozygous hypobetalipoproteinemia should be ruled out in patients with unexplained hepatic steatosis.
AuthorsG Castellano, C Garfia, D Gomez-Coronado, J Arenas, J Manzanares, F Colina, J A Solis-Herruzo
JournalJournal of clinical gastroenterology (J Clin Gastroenterol) Vol. 25 Issue 1 Pg. 379-82 (Jul 1997) ISSN: 0192-0790 [Print] United States
PMID9412928 (Publication Type: Case Reports, Journal Article)
Topics
  • Adult
  • Biopsy
  • Fatty Liver (complications, diagnostic imaging, pathology)
  • Heterozygote
  • Humans
  • Hypobetalipoproteinemias (etiology, genetics, pathology)
  • Male
  • Ultrasonography

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: