[Usefulness of a diagnostic algorithm hyperferritinemia: A case report of a Spanish family with hereditary hemochromatosis and mutation in SLC40A1 gene]

Med Clin (Barc). 2015 Jul 6;145(1):42-3. doi: 10.1016/j.medcli.2014.09.001. Epub 2014 Nov 24.
[Article in Spanish]
No abstract available

Publication types

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

MeSH terms

  • Algorithms
  • Cation Transport Proteins / deficiency
  • Cation Transport Proteins / genetics*
  • DNA Mutational Analysis
  • Female
  • Ferritins / blood*
  • Ferroportin
  • Genotype
  • Hemochromatosis / diagnosis
  • Hemochromatosis / genetics*
  • Humans
  • Iron / blood
  • Liver / pathology
  • Magnetic Resonance Imaging
  • Male
  • Middle Aged
  • Spain
  • Transferrin / analysis

Substances

  • Cation Transport Proteins
  • Transferrin
  • Ferroportin
  • Ferritins
  • Iron