Etiology (exemples)

 nonalcoholic fatty liver disease (NAFLD)

• genetic metabolic diseases (inborn errors of metabolism)
  • hereditary fructose intolerance
  • galactosemia
  • glycogen storage disease type I (GSD1)
  • glycogen storage disease type II (GSD2)
  • Wolman disease
  • cholesterol ester storage disease
  • mitochondrial respiratory chain diseases
  • fatty acid oxydation diseases
  • pyruvate carboxylase deficiency
  • pyruvate dehydrogenasedeficiency
  • neonatal adrenoleukodystrophy
  • infantile Refsum disease
  • herediatry tyrosinemia
  • Wilson disease
  • organic acidurias
  • urea cycle diseases

 nonalcoholic steatohepatitis (NASH)

See also

 steatohepatitis

• alcoholic steatohepatitis
• non-alcoholic steatohepatitis

References

 Zafrani ES. Non-alcoholic fatty liver disease: an emerging pathological spectrum. Virchows Arch. 2004 Jan;444(1):3-12. PMID: #14685853#

 Burt AD, Mutton A, Day CP. Diagnosis and interpretation of steatosis and steatohepatitis. Semin Diagn Pathol. 1998 Nov;15(4):246-58. PMID: #9845426#