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Hereditary xerocytosis. A case history and review of the literature.

Abstract
A case of hereditary xerocytosis, a rare hemolytic anemia with dehydrated erythrocytes resulting from excess potassium efflux through the red cell membrane, is presented and the literature on the subject reviewed. This is one of the first cases reported from Australia.
AuthorsG R Nolan
JournalPathology (Pathology) Vol. 16 Issue 2 Pg. 151-4 (Apr 1984) ISSN: 0031-3025 [Print] England
PMID6462778 (Publication Type: Case Reports, Journal Article)
Chemical References
  • Diphosphoglyceric Acids
  • Electrolytes
  • Enzymes
  • 2,3-Diphosphoglycerate
Topics
  • 2,3-Diphosphoglycerate
  • Adult
  • Anemia, Hemolytic, Congenital (genetics)
  • Anemia, Hemolytic, Congenital Nonspherocytic (enzymology, genetics)
  • Cell Membrane Permeability
  • Diphosphoglyceric Acids (blood)
  • Electrolytes (blood)
  • Enzymes (blood)
  • Erythrocyte Count
  • Erythrocyte Indices
  • Erythrocytes (enzymology)
  • Hemoglobinometry
  • Humans
  • Male

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