Literature DB >> 1398867

Effect of G-6 PD deficiency on sickle cell disease in Saudi Arabia.

B H Awamy1.   

Abstract

High incidence of G6PD deficiency has been reported in areas of the eastern province of Saudi Arabia where sickle cell gene is also prevalent. This study was conducted to assess the co-incidence of this enzymopathy with Hb S and its influence upon the clinical and hematological expression of sickle cell disease. Eighty three children with SS disease, 145 patients with sickle cell trait and 100 random cord blood as samples with normal Hb AF, and an FS electrophoretic pattern respectively were examined. The frequency of interaction of G6PD deficiency with Hb S was found significantly increased but no effect of this enzyme defect was discerned on the clinical and hematological status of homozygous sickle cell disease.

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Year:  1992        PMID: 1398867     DOI: 10.1007/bf02821799

Source DB:  PubMed          Journal:  Indian J Pediatr        ISSN: 0019-5456            Impact factor:   1.967


  11 in total

1.  CORRELATION OF S HEMOGLOBIN WITH GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY AND ITS SIGNIFICANCE.

Authors:  R A LEWIS; M HATHORN
Journal:  Blood       Date:  1965-08       Impact factor: 22.113

2.  Sex-linked electrophoretic difference in glucose-6-phosphate dehydrogenase.

Authors:  H N KIRKMAN; E M HENDRICKSON
Journal:  Am J Hum Genet       Date:  1963-09       Impact factor: 11.025

3.  Glucose-6-phosphate dehydrogenase deficiency in red blood cells of East Africans.

Authors:  A C ALLISON
Journal:  Nature       Date:  1960-05-14       Impact factor: 49.962

4.  Activity of glucose-6-phosphate dehydrogenase in erythrocyes of patients with various abnormal hemoglobins.

Authors:  J NAYLOR; I ROSENTHAL; A GROSSMAN; I SCHULMAN; D Y HSIA
Journal:  Pediatrics       Date:  1960-08       Impact factor: 7.124

5.  Simplified method for G6PD screening using blood collected on filter paper.

Authors:  P A Dow; M B Petteway; J B Alperin
Journal:  Am J Clin Pathol       Date:  1974-03       Impact factor: 2.493

6.  Reliable routine estimation of small amounts of foetal haemoglobin by alkali denaturation.

Authors:  M E Pembrey; P McWade; D J Weatherall
Journal:  J Clin Pathol       Date:  1972-08       Impact factor: 3.411

7.  The hemolytic crisis of sickle cell disease: the role of glucose-6-phosphate dehydrogenase deficiency.

Authors:  H L Smits; F A Oski; J I Brody
Journal:  J Pediatr       Date:  1969-04       Impact factor: 4.406

8.  Neonatal screening for sickle cell disease in the Eastern Province of Saudi Arabia.

Authors:  B H Al-Awamy; M Al-Muzan; M Al-Turki; G R Serjeant
Journal:  Trans R Soc Trop Med Hyg       Date:  1984       Impact factor: 2.184

9.  Glucose-6-phosphate dehydrogenase deficiency and homozygous sickle cell disease in Jamaica.

Authors:  W N Gibbs; J Wardle; G R Serjeant
Journal:  Br J Haematol       Date:  1980-05       Impact factor: 6.998

10.  Haemoglobin disorders: a pattern for thalassaemia and haemoglobinopathies in Arabia.

Authors:  M A El-Hazmi
Journal:  Acta Haematol       Date:  1982       Impact factor: 2.195

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