Literature DB >> 11533744

Thalassemia syndromes in Saudi Arabia. Meta-analysis of local studies.

B H Al-Awamy1.   

Abstract

The geographical distribution of Alpha and Beta-Thalassemias differ markedly. Alpha-Thalassemia being particularly prevalent in Southeast Asia and Beta-Thalassemia in the Mediterranean basin. Thalassemia syndromes are common in Saudi Arabia: the Beta-Thalassemia genes occur with variable frequency in different regions of Saudi Arabia and both B+ and Bo thalassemia have been reported. Alpha-Thalassemia is also highly prevalent here and the interaction with the sickle cell gene is commonly observed. Over the last few years, a great deal of information regarding the clinical, molecular and management of these disorders has accumulated in the literature. In this paper we summarize some of the recent studies on the subject along with our experience and our attempt to highlight a number of questions still awaiting answers.

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Year:  2000        PMID: 11533744

Source DB:  PubMed          Journal:  Saudi Med J        ISSN: 0379-5284            Impact factor:   1.484


  17 in total

1.  Epidemiological profile of common haemoglobinopathies in Arab countries.

Authors:  Hanan A Hamamy; Nasir A S Al-Allawi
Journal:  J Community Genet       Date:  2012-12-08

2.  Homozygosity for the Mediterranean a-thalassemic deletion (hemoglobin Barts hydrops fetalis).

Authors:  Nasir A S Al-Allawi; Maida Y Shamdeen; Najeeb S Rasheed
Journal:  Ann Saudi Med       Date:  2010 Mar-Apr       Impact factor: 1.526

3.  Prevalence of beta-thalassemia trait in premarital screening in Al-Hassa, Saudi Arabia.

Authors:  Ahmad Al-Suliman
Journal:  Ann Saudi Med       Date:  2006 Jan-Feb       Impact factor: 1.526

4.  Measurement of reticulocyte hemoglobin content to diagnose iron deficiency in Saudi children.

Authors:  Ahmad Fayez Bakr; Gale Sarette
Journal:  Eur J Pediatr       Date:  2006-03-07       Impact factor: 3.183

5.  A comparative study of hematological parameters of α and β thalassemias in a high prevalence zone: Saudi Arabia.

Authors:  Syed Riaz Mehdi; Badr Abdullah Al Dahmash
Journal:  Indian J Hum Genet       Date:  2011-09

Review 6.  Genetic epidemiology of hemoglobinopathies among Iraqi Kurds.

Authors:  Nasir Al-Allawi; Sarah Al Allawi; Sana D Jalal
Journal:  J Community Genet       Date:  2020-11-22

7.  Incidence of alpha-globin gene defect in the Lebanese population: a pilot study.

Authors:  Chantal Farra; Rose Daher; Rebecca Badra; Rym el Rafei; Rachelle Bejjany; Lama Charafeddine; Khalid Yunis
Journal:  Biomed Res Int       Date:  2015-03-05       Impact factor: 3.411

8.  Spectral detection of thalassemia: a preliminary study.

Authors:  M S Alsalhi; Farjah H Algahtani; S Devanesan; V Trinka Vijmasi; K Jeyaprakash; Abbas H Alsaeed; V Masilamani
Journal:  J Biomed Sci       Date:  2014-03-29       Impact factor: 8.410

9.  Analysis of hemoglobin electrophoresis results and physicians investigative practices in Saudi Arabia.

Authors:  Syed Riaz Mehdi; Badr Abdullah Al Dahmash
Journal:  Indian J Hum Genet       Date:  2013-07

10.  The prevalence of anemia and hemoglobinopathies in the hematologic clinics of the kermanshah province, Western iran.

Authors:  Mehrdad Payandeh; Zohreh Rahimi; Mohammad Erfan Zare; Atefeh Nasir Kansestani; Farzad Gohardehi; Amir Hossein Hashemian
Journal:  Int J Hematol Oncol Stem Cell Res       Date:  2014
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