Fatty liver in H63D homozygotes with hyperferritinemia

World J Gastroenterol. 2006 Mar 21;12(11):1788-92. doi: 10.3748/wjg.v12.i11.1788.

Abstract

To study the clinical correlates of the H63D mutation we have analysed the phenotype of H63D homo-zygotes identified through mutation analysis in a referral laboratory. A total of 366 blood samples referred for HFE analysis were screened for C282Y and H63D mutations. Four H63D homozygotes were identified. All had raised serum ferritin but normal transferrin saturation. They were negative for hepatitis B and C and only one patient consumed excess alcohol. In all 4 cases ultrasonography revealed fatty liver. In two patients a liver biopsy was done and showed mild siderosis with an unusual distribution and macrovesicular steatosis. These data confirm the association between fatty liver, hyperferritinaemia and increased hepatic iron, but do not clarify whether siderosis was related to steatosis rather than homozygosity for the H63D mutation. Patients with fatty liver may complicate the interpretation of data in population studies of the expression of H63D homozygosity.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Aged
  • Fatty Liver / blood
  • Fatty Liver / diagnosis*
  • Fatty Liver / genetics
  • Fatty Liver / pathology
  • Ferritins / blood*
  • Hemochromatosis / genetics*
  • Hemochromatosis Protein
  • Histocompatibility Antigens Class I / genetics*
  • Homozygote
  • Humans
  • Iron / analysis
  • Liver / chemistry
  • Liver / diagnostic imaging
  • Liver / pathology
  • Male
  • Membrane Proteins / genetics*
  • Mutation, Missense
  • Siderosis / diagnosis
  • Siderosis / pathology
  • Ultrasonography

Substances

  • HFE protein, human
  • Hemochromatosis Protein
  • Histocompatibility Antigens Class I
  • Membrane Proteins
  • Ferritins
  • Iron