Literature DB >> 6181641

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

M A El-Hazmi.   

Abstract

The mild course of the diseased state of haemoglobinopathies and the thalassaemias in Arabia and the interaction of the genetic abnormality and environmental factors are particularly interesting as the Peninsula exhibits a diverse climate and topography that encourages study of the interactions between various genetic and environmental factors. The present study is aimed at elucidating the incidence and frequency of these genetic abnormalities in various regions of Saudi Arabia. The relationship between haemoglobinopathies, thalassaemia and glucose-6-phosphate dehydrogenase deficiency on the one hand and malaria parasites on the other are elucidated. The results are presented in the light of the environmental factors prevailing in the area.

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Year:  1982        PMID: 6181641     DOI: 10.1159/000206947

Source DB:  PubMed          Journal:  Acta Haematol        ISSN: 0001-5792            Impact factor:   2.195


  14 in total

1.  Leftward deletion alpha-thalassaemia in the Saudi Arabian population.

Authors:  M A el-Hazmi
Journal:  Hum Genet       Date:  1986-11       Impact factor: 4.132

2.  Alpha-thalassemia in Saudi Arabia: deletion pattern.

Authors:  M A el-Hazmi
Journal:  Hum Genet       Date:  1987-06       Impact factor: 4.132

3.  Consanguinity among the Saudi Arabian population.

Authors:  M A el-Hazmi; A R al-Swailem; A S Warsy; A M al-Swailem; R Sulaimani; A A al-Meshari
Journal:  J Med Genet       Date:  1995-08       Impact factor: 6.318

4.  Clinical and Therapeutic Profiles of Heart Failure Patients admitted to a Tertiary Hospital, Aseer Region, Saudi Arabia.

Authors:  Abdullah S Assiri
Journal:  Sultan Qaboos Univ Med J       Date:  2011-05-15

5.  Beta-globin gene polymorphism in the Saudi Arab population.

Authors:  M A el-Hazmi
Journal:  Hum Genet       Date:  1986-05       Impact factor: 4.132

Review 6.  Differences in the clinical and genotypic presentation of sickle cell disease around the world.

Authors:  Santosh L Saraf; Robert E Molokie; Mehdi Nouraie; Craig A Sable; Lori Luchtman-Jones; Gregory J Ensing; Andrew D Campbell; Sohail R Rana; Xiao M Niu; Roberto F Machado; Mark T Gladwin; Victor R Gordeuk
Journal:  Paediatr Respir Rev       Date:  2013-11-15       Impact factor: 2.726

7.  Red cell parameters in infant and children from the Arabian Peninsula.

Authors:  Lolowa A Al Mekaini; Srdjan Denic; Omar N Al Jabri; Hassib Narchi; Abdul-Kader Souid; Suleiman Al-Hammadi
Journal:  Am J Blood Res       Date:  2015-12-25

8.  Decline in hepatitis B infection in sickle cell anaemia and beta thalassaemia major.

Authors:  I al-Fawaz; S Ramia
Journal:  Arch Dis Child       Date:  1993-11       Impact factor: 3.791

9.  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

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

Authors:  B H Awamy
Journal:  Indian J Pediatr       Date:  1992 May-Jun       Impact factor: 1.967

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