Literature DB >> 10050708

A variant of hereditary stomatocytosis with marked pseudohyperkalaemia.

S E Coles1, M M Ho, M C Chetty, A Nicolaou, G W Stewart.   

Abstract

A family with an unusual form of hereditary stomatocytosis is described. The affected members showed a mild, dominantly-inherited, haemolytic anaemia with intracellular Na and K levels of 41-48 and 44-53 mmol/(l cells) respectively. This anaemia was associated with marked 'pseudohyperkalaemia': that is, loss of K from red cells on storage at room temperature. At 37 degrees C, 'leak' tracer flux rates (assessed as the ouabain + bumetanide-resistant K fluxes) showed a roughly 5-fold acceleration compared to normal, and an abnormal temperature dependence with a shallow slope between 37 and 20 degrees C (mean Q10 (ratio of reaction rates at temperature T and T - 10) over this interval, 1.6; normal 2.2). The pseudohyperkalaemia could be attributed to the disparity between pump and leak at 20 degrees C. This is an identical mechanism to that previously shown for the haemato logically trivial condition, 'familial pseudohyperkalaemia. No protein or lipid abnormality was found in the membrane of these cells.

Entities:  

Mesh:

Substances:

Year:  1999        PMID: 10050708     DOI: 10.1046/j.1365-2141.1999.01191.x

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


  10 in total

1.  A family showing recessively inherited multisystem pathology with aberrant splicing of the erythrocyte Band 7.2b ('stomatin') gene.

Authors:  A C Argent; M C Chetty; B Fricke; Y Bertrand; N Philippe; S Khogali; M von Düring; J Delaunay; G W Stewart
Journal:  J Inherit Metab Dis       Date:  2004       Impact factor: 4.982

Review 2.  Disorders of erythrocyte volume homeostasis.

Authors:  E Glogowska; P G Gallagher
Journal:  Int J Lab Hematol       Date:  2015-05       Impact factor: 2.877

Review 3.  Disorders of erythrocyte hydration.

Authors:  Patrick G Gallagher
Journal:  Blood       Date:  2017-10-19       Impact factor: 22.113

Review 4.  Determinants of erythrocyte hydration.

Authors:  Jesse Rinehart; Erol E Gulcicek; Clinton H Joiner; Richard P Lifton; Patrick G Gallagher
Journal:  Curr Opin Hematol       Date:  2010-05       Impact factor: 3.284

Review 5.  Temperature effects on cation transport in hereditary stomatocytosis and allied disorders.

Authors:  S E Coles; G W Stewart
Journal:  Int J Exp Pathol       Date:  1999-10       Impact factor: 1.925

6.  A novel erythroid anion exchange variant (Gly796Arg) of hereditary stomatocytosis associated with dyserythropoiesis.

Authors:  Achille Iolascon; Luigia De Falco; Franck Borgese; Maria Rosaria Esposito; Rosa Anna Avvisati; Pietro Izzo; Carmelo Piscopo; Helene Guizouarn; Andrea Biondani; Antonella Pantaleo; Lucia De Franceschi
Journal:  Haematologica       Date:  2009-08       Impact factor: 9.941

7.  Methyl-beta-cyclodextrin stimulates glucose uptake in Clone 9 cells: a possible role for lipid rafts.

Authors:  Kay Barnes; Jean C Ingram; Matthew D M Bennett; Gordon W Stewart; Stephen A Baldwin
Journal:  Biochem J       Date:  2004-03-01       Impact factor: 3.857

Review 8.  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

9.  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

Review 10.  Review. Leaky Cl--HCO3- exchangers: cation fluxes via modified AE1.

Authors:  J C Ellory; H Guizouarn; F Borgese; L J Bruce; R J Wilkins; G W Stewart
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2009-01-27       Impact factor: 6.237

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.