Literature DB >> 11167849

Familial pseudohyperkalaemia Chiswick: a novel congenital thermotropic variant of K and Na transport across the human red cell membrane.

P G Haines1, C Crawley, M C Chetty, H Jarvis, S E Coles, J Fisher, A Nicolaou, G W Stewart.   

Abstract

Two families with inherited abnormalities in Na and K transport across the red cell membrane are described. Both presented with 'pseudohyperkalaemia' as a result of loss of K from the red cells on storage at room temperature. Routine haematology was essentially normal, except for macrocytosis in one family. Studies of the temperature dependence of the passive leak to K showed a novel shoulder pattern with a minimum at 25 degrees C, a maximum at 10 degrees C, followed by a further fall. As in other cases of red cell-based pseudohyperkalaemia, the abnormal temperature dependence of this 'leak' flux could be held to account for the loss of K from the cells at room temperature. These cases represent a novel variant of the temperature dependence of the passive leak of K and Na across the red cell membrane, and can be classified as a mild, non-haemolytic form of the group known as the hereditary stomatocytosis and allied disorders'.

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Year:  2001        PMID: 11167849     DOI: 10.1046/j.1365-2141.2001.02564.x

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


  4 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

2.  Functional characterization of novel ABCB6 mutations and their clinical implications in familial pseudohyperkalemia.

Authors:  Immacolata Andolfo; Roberta Russo; Francesco Manna; Gianluca De Rosa; Antonella Gambale; Soha Zouwail; Nicola Detta; Catia Lo Pardo; Seth L Alper; Carlo Brugnara; Alok K Sharma; Lucia De Franceschi; Achille Iolascon
Journal:  Haematologica       Date:  2016-05-05       Impact factor: 9.941

Review 3.  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

4.  Atypical hereditary spherocytosis phenotype associated with pseudohypokalaemia and a new variant in the band 3 protein.

Authors:  Indra Ramasamy
Journal:  BMJ Case Rep       Date:  2020-12-09
  4 in total

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