Hereditary xerocytosis: Diagnostic considerations

Am J Hematol. 2018 Mar;93(3):E67-E69. doi: 10.1002/ajh.24996. Epub 2017 Dec 23.
No abstract available

Publication types

  • Letter
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Substitution*
  • Anemia, Hemolytic, Congenital / blood
  • Anemia, Hemolytic, Congenital / complications
  • Anemia, Hemolytic, Congenital / diagnosis*
  • Anemia, Hemolytic, Congenital / genetics
  • Cholelithiasis / complications
  • Conserved Sequence
  • Erythrocyte Deformability
  • Erythrocyte Indices
  • Female
  • Hemoglobins / analysis
  • Humans
  • Hydrops Fetalis / blood
  • Hydrops Fetalis / diagnosis*
  • Hydrops Fetalis / etiology
  • Hydrops Fetalis / genetics
  • Ion Channels / chemistry
  • Ion Channels / genetics*
  • Ion Channels / physiology
  • Jaundice, Neonatal / etiology
  • Male
  • Mutation, Missense*
  • Pedigree
  • Phenotype
  • Reticulocyte Count

Substances

  • Hemoglobins
  • Ion Channels
  • PIEZO1 protein, human

Supplementary concepts

  • Xerocytosis, hereditary