Literature DB >> 892808

New data on glucose-6-phosphate dehydrogenase deficiency in Saudi Arabia. G6PD variants, and the association between enzyme deficiency and hemoglobins S.

A P Gelpi, M C King.   

Abstract

67/369 male Saudi subjects (18%) were found to be G6PD deficient on screening, and electrophoresis of blood samples stored on filter paper strips revealed B-like variants with intermediate enzyme activityin 11%, presumed Mediterranean variant in 13%, Gd + (A+) in 2%, Gd--(A--7) in 0.8%, and indeterminate enzyme status in 6% of the subjects tested. A significant association between G6PD deficiency and hemoglobin S correlated with previous studies on similar samples from the general population.

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Year:  1977        PMID: 892808     DOI: 10.1159/000152880

Source DB:  PubMed          Journal:  Hum Hered        ISSN: 0001-5652            Impact factor:   0.444


  3 in total

1.  6-Phosphogluconolactonase deficiency, a hereditary erythrocyte enzyme deficiency: possible interaction with glucose-6-phosphate dehydrogenase deficiency.

Authors:  E Beutler; W Kuhl; T Gelbart
Journal:  Proc Natl Acad Sci U S A       Date:  1985-06       Impact factor: 11.205

2.  Aspects of sickle cell gene in Saudi Arabia--interaction with glucose-6-phosphate dehydrogenase deficiency.

Authors:  M A el-Hazmi; A S Warsy
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

3.  Origin and spread of the glucose-6-phosphate dehydrogenase variant (G6PD-Mediterranean) in the Middle East.

Authors:  B Kurdi-Haidar; P J Mason; A Berrebi; G Ankra-Badu; A al-Ali; A Oppenheim; L Luzzatto
Journal:  Am J Hum Genet       Date:  1990-12       Impact factor: 11.025

  3 in total

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