Literature DB >> 7336156

High prevalence of increased osmotic fragility of red blood cells among Norwegian blood donors.

H C Godal, H Heistø.   

Abstract

Increased osmotic fragility of red blood cells was found in 9 out of 1008 Norwegian blood donors. In addition, increased osmotic fragility was found in 3 out of 23 first grade relatives and in 1 out of 4 spouses of individuals with the same condition. Finally, there was a positive correlation between increased osmotic fragility and morphological signs of spherocytosis (P less than 0.05). No definite conclusions with respect to underlying mechanism(s) for this high prevalence of non-symptomatic increased osmotic fragility can be offered, but very mild hereditary spherocytosis, environmental factors and even a normal variant, never associated with haemolysis, may have contributed. Furthermore, until more specific and sensitive laboratory techniques have been introduced, a proper distinction between these 3 conditions cannot be made.

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Mesh:

Year:  1981        PMID: 7336156     DOI: 10.1111/j.1600-0609.1981.tb00448.x

Source DB:  PubMed          Journal:  Scand J Haematol        ISSN: 0036-553X


  15 in total

1.  Spectrin/band 3 ratio as diagnostic tool in hereditary spherocytosis.

Authors:  S Cutillo; L Pinto; B Nobili; E Miraglia del Giudice; A Iolascon
Journal:  Eur J Pediatr       Date:  1992-01       Impact factor: 3.183

2.  Functional analysis of a novel cis-acting regulatory region within the human ankyrin gene (ANK-1) promoter.

Authors:  Karina Laflamme; Ashley N Owen; Emily E Devlin; Mary Q Yang; Clara Wong; Laurie A Steiner; Lisa J Garrett; Laura Elnitski; Patrick G Gallagher; David M Bodine
Journal:  Mol Cell Biol       Date:  2010-05-17       Impact factor: 4.272

3.  A systematic review of hereditary spherocytosis reported in Chinese biomedical journals from 1978 to 2013 and estimation of the prevalence of the disease using a disease model.

Authors:  Chao Wang; Yazhou Cui; Yan Li; Xiao Liu; Jinxiang Han
Journal:  Intractable Rare Dis Res       Date:  2015-05

4.  The clinical relevance of an isolated increase in the number of circulating hyperchromic red blood cells.

Authors:  A M Conway; A J Vora; R F Hinchliffe
Journal:  J Clin Pathol       Date:  2002-11       Impact factor: 3.411

5.  Proteomic identification of erythrocyte membrane protein deficiency in hereditary spherocytosis.

Authors:  Selen Peker; Nejat Akar; Duygu Ozel Demiralp
Journal:  Mol Biol Rep       Date:  2011-06-26       Impact factor: 2.316

6.  Prevalence of increased osmotic fragility of erythrocytes in German blood donors: screening using a modified glycerol lysis test.

Authors:  S W Eber; A Pekrun; A Neufeldt; W Schröter
Journal:  Ann Hematol       Date:  1992-02       Impact factor: 3.673

7.  Hereditary spherocytosis in a malay patient with chronic haemolysis.

Authors:  Muhammad Kamil Sheikh; Narazah Mohd Yusoff; Gurjeet Kaur; Farhat Aziz Khan
Journal:  Malays J Med Sci       Date:  2007-07

Review 8.  Erythrocyte disorders in the perinatal period.

Authors:  Laurie A Steiner; Patrick G Gallagher
Journal:  Semin Perinatol       Date:  2007-08       Impact factor: 3.300

9.  Oxidative stress and histopathological changes induced by methylthiophanate, a systemic fungicide, in blood, liver and kidney of adult rats.

Authors:  Ben Amara Ibtissem; Ben Saad Hajer; Hakim Ahmed; Elwej Awatef; Kallel Choumous; Boudawara Ons; Zeghal Khaled Mounir; Zeghal Najiba
Journal:  Afr Health Sci       Date:  2017-03       Impact factor: 0.927

10.  Identification of a novel p.Q1772X ANK1 mutation in a Korean family with hereditary spherocytosis.

Authors:  Joo Hyung Han; Seung Kim; Hoon Jang; So Won Kim; Min Goo Lee; Hong Koh; Ji Hyun Lee
Journal:  PLoS One       Date:  2015-06-24       Impact factor: 3.240

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