A Rare Case Of a 2-year-old Boy With Alagille Syndrome and Type 3 Hereditary Hemochromatosis With TFR2 Mutation

J Pediatr Gastroenterol Nutr. 2019 Apr;68(4):e68-e70. doi: 10.1097/MPG.0000000000002078.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Alagille Syndrome / blood
  • Alagille Syndrome / complications
  • Alagille Syndrome / diagnosis*
  • Hemochromatosis / blood
  • Hemochromatosis / complications
  • Hemochromatosis / diagnosis*
  • Hispanic or Latino
  • Humans
  • Infant
  • Male
  • Mutation
  • Receptors, Transferrin / blood
  • Receptors, Transferrin / deficiency*
  • Receptors, Transferrin / genetics

Substances

  • Receptors, Transferrin
  • TFR2 protein, human

Supplementary concepts

  • Hemochromatosis, type 3