Four pedigrees of the cation-leaky hereditary stomatocytosis class presenting with pseudohyperkalaemia. Novel profile of temperature dependence of Na+-K+ leak in a xerocytic form
- PMID: 15142123
- DOI: 10.1111/j.1365-2141.2004.04944.x
Four pedigrees of the cation-leaky hereditary stomatocytosis class presenting with pseudohyperkalaemia. Novel profile of temperature dependence of Na+-K+ leak in a xerocytic form
Abstract
We report four pedigrees of the group of Na(+)-K(+)-leaky red cell disorders of the 'hereditary stomatocytosis' class. Each showed pseudohyperkalaemia because of temperature-dependent loss of K(+) from red cells on storage of whole blood at room temperature. All pedigrees showed an abnormality in the temperature dependence of the 'passive leak' of the membrane to K(+). Two pedigrees, both of which showed a compensated haemolytic state with dehydrated red cells and target cells on the blood film, showed a novel pattern, in which the profile was flat between 37 degrees C and about 32 degrees C then dropped as the temperature was reduced to zero. The third showed the 'shallow slope' profile, with stomatocytes on the blood film and very markedly abnormal intracellular Na(+) and K(+) levels. Minimal haemolysis was present. The fourth pedigree, of Asian origin, showed the shoulder pattern (minimum at 32 degrees C, maximum at 12 degrees C) with essentially normal haematology. Both of these latter two forms have previously been seen in other pedigrees. The first variant represents a novel kind of temperature dependence of the passive leak found in these pedigrees presenting with pseudohyperkalaemia.
Similar articles
-
Familial pseudohyperkalaemia Chiswick: a novel congenital thermotropic variant of K and Na transport across the human red cell membrane.Br J Haematol. 2001 Feb;112(2):469-74. doi: 10.1046/j.1365-2141.2001.02564.x. Br J Haematol. 2001. PMID: 11167849
-
Four new cases of stomatin-deficient hereditary stomatocytosis syndrome: association of the stomatin-deficient cryohydrocytosis variant with neurological dysfunction.Br J Haematol. 2004 Jun;125(6):796-803. doi: 10.1111/j.1365-2141.2004.04965.x. Br J Haematol. 2004. PMID: 15180870
-
Pseudohyperkalaemia and pseudomacrocytosis caused by inherited red-cell disorders of the 'hereditary stomatocytosis' group.Br J Biomed Sci. 2001;58(1):48-55. Br J Biomed Sci. 2001. PMID: 11284226 Review.
-
South-east Asian ovalocytosis and the cryohydrocytosis form of hereditary stomatocytosis show virtually indistinguishable cation permeability defects.Br J Haematol. 2011 Mar;152(5):655-64. doi: 10.1111/j.1365-2141.2010.08454.x. Epub 2011 Jan 23. Br J Haematol. 2011. PMID: 21255002
-
Hereditary stomatocytosis and cation-leaky red cells--recent developments.Blood Cells Mol Dis. 2009 May-Jun;42(3):216-22. doi: 10.1016/j.bcmd.2009.01.014. Epub 2009 Mar 3. Blood Cells Mol Dis. 2009. PMID: 19261491 Review.
Cited by
-
Cryohydrocytosis: increased activity of cation carriers in red cells from a patient with a band 3 mutation.Haematologica. 2010 Feb;95(2):189-98. doi: 10.3324/haematol.2009.010215. Epub 2009 Dec 16. Haematologica. 2010. PMID: 20015879 Free PMC article.
-
Dehydrated hereditary stomatocytosis: clinical perspectives.J Blood Med. 2019 Jul 4;10:183-191. doi: 10.2147/JBM.S179764. eCollection 2019. J Blood Med. 2019. PMID: 31308777 Free PMC article.
-
The Molecular Basis for Altered Cation Permeability in Hereditary Stomatocytic Human Red Blood Cells.Front Physiol. 2018 Apr 16;9:367. doi: 10.3389/fphys.2018.00367. eCollection 2018. Front Physiol. 2018. PMID: 29713289 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Molecular Biology Databases