Literature DB >> 10216110

Familial pseudohyperkalemia maps to the same locus as dehydrated hereditary stomatocytosis (hereditary xerocytosis).

A Iolascon1, G W Stewart, J F Ajetunmobi, S Perrotta, J Delaunay, M Carella, L Zelante, P Gasparini.   

Abstract

Familial pseudohyperkalemia is a "leaky red blood cell" condition in which the cells show a temperature-dependent loss of potassium (K) from red blood cells when stored at room temperature, manifesting as apparent hyperkalemia. The red blood cells show a reduced lifespan in vivo but there is no frank hemolysis. Studies of cation content and transport show a marginal increase in permeability at 37 degrees C and a degree of cellular dehydration, qualitatively similar to the changes seen in dehydrated hereditary stomatocytosis (hereditary xerocytosis). Physiological studies have shown that the passive leak to K has an abnormal temperature dependence, such that the leak is less sensitive to temperature than that in normal cells. We performed genetic mapping on the original family and found that the condition in this kindred maps to the same locus (16q23-ter) that we have previously identified for an Irish family with dehydrated hereditary stomatocytosis, which does not show the same temperature effects.

Entities:  

Mesh:

Substances:

Year:  1999        PMID: 10216110

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  10 in total

1.  The hereditary stomatocytoses.

Authors:  Joanna F Flatt; Lesley J Bruce
Journal:  Haematologica       Date:  2009-08       Impact factor: 9.941

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

5.  Mutations in the mechanotransduction protein PIEZO1 are associated with hereditary xerocytosis.

Authors:  Ryan Zarychanski; Vincent P Schulz; Brett L Houston; Yelena Maksimova; Donald S Houston; Brian Smith; Jesse Rinehart; Patrick G Gallagher
Journal:  Blood       Date:  2012-04-23       Impact factor: 22.113

6.  Reversible iatrogenic paraparesis secondary to masked hypokalaemia in thrombocytosis-associated pseudohyperkalaemia.

Authors:  Ina Dubin; Ami Schattner
Journal:  BMJ Case Rep       Date:  2019-03-22

Review 7.  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

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.  A case of severe pseudohyperkalaemia due to muscle contraction.

Authors:  Jan Van Elslande; Toon Dominicus; Jaan Toelen; Glynis Frans; Pieter Vermeersch
Journal:  Biochem Med (Zagreb)       Date:  2020-06-15       Impact factor: 2.313

Review 10.  Congenital Hemolytic Anemias: Is There a Role for the Immune System?

Authors:  Anna Zaninoni; Elisa Fermo; Cristina Vercellati; Anna Paola Marcello; Wilma Barcellini; Paola Bianchi
Journal:  Front Immunol       Date:  2020-06-23       Impact factor: 7.561

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.