Literature DB >> 11918557

Familial pseudohyperkalaemia Cardiff: a mild version of cryohydrocytosis.

Daniel M Gore1, Margaret C Chetty, Julie Fisher, Anna Nicolaou, Gordon W Stewart.   

Abstract

We have investigated a Welsh pedigree showing the 'familial pseudohyperkalaemia' phenotype of dominantly inherited, red-cell-based, temperature-dependent pseudohyperkalaemia associated with normal haematology. The 'passive leak' to K across the membrane of these abnormal red cells showed a 'U-shaped' temperature dependence, with a minimum at about 23 degrees C, qualitatively similar to that seen in the frankly haemolytic 'cryohydrocytosis' variant of the hereditary stomatocytosis group. Like three previous pedigrees with cryohydrocytosis, these patients show an excess of ether lipids in the membrane. However, these patients differ from other 'familial pseudohyperkalaemia' pedigrees, in which the leak showed different temperature profiles.

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Year:  2002        PMID: 11918557     DOI: 10.1046/j.1365-2141.2002.03376.x

Source DB:  PubMed          Journal:  Br J Haematol        ISSN: 0007-1048            Impact factor:   6.998


  2 in total

1.  Cryohydrocytosis: increased activity of cation carriers in red cells from a patient with a band 3 mutation.

Authors:  Anna Bogdanova; Jeroen S Goede; Erwin Weiss; Nikolay Bogdanov; Poul Bennekou; Ingolf Bernhardt; Hans U Lutz
Journal:  Haematologica       Date:  2009-12-16       Impact factor: 9.941

Review 2.  The Molecular Basis for Altered Cation Permeability in Hereditary Stomatocytic Human Red Blood Cells.

Authors:  Joanna F Flatt; Lesley J Bruce
Journal:  Front Physiol       Date:  2018-04-16       Impact factor: 4.566

  2 in total

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