Severe steatohepatitis in a patient with a rare neutral lipid storage disorder due to ABHD5 mutation

J Hepatol. 2008 Sep;49(3):474-7. doi: 10.1016/j.jhep.2008.05.027. Epub 2008 Jul 9.

Abstract

Fatty liver disease is mainly caused by alcohol consumption, excessive body weight, dyslipidemia and impaired glucose tolerance, but inherited disorders can sometimes be involved. We report the case of a 40-year-old woman with steatohepatitis and severe portal hypertension, associated with ichthyosis, cataract and hypoacusia. The clinical, pathological and genetic findings were consistent with a diagnosis of Chanarin-Dorfman syndrome (CDS), a rare autosomal recessive inherited neutral lipid storage disorder, and genetic analysis showed that a novel ABHD5 mutation is responsible.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • 1-Acylglycerol-3-Phosphate O-Acyltransferase
  • Adult
  • Fatty Liver / diagnosis*
  • Fatty Liver / etiology*
  • Female
  • Hepatitis / diagnosis*
  • Hepatitis / etiology*
  • Humans
  • Lipase / genetics*
  • Lipid Metabolism Disorders / complications*
  • Lipid Metabolism Disorders / genetics*
  • Liver / pathology
  • Mutation / genetics

Substances

  • 1-Acylglycerol-3-Phosphate O-Acyltransferase
  • ABHD5 protein, human
  • Lipase