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Beta Thalassemia Frequency in Bahrain: A Ten Year Study

 
 

Date   :  27-09-2010

Visits  : 106  
 

Attachments : لا يوجد

Descripiton :

 
 

 

to see the full research please click in the link below

للاطلاع على البحث بالكامل الرجاء الضغط على الرابط ادناه

http://www.bahrainmedicalbulletin.com/june_2010/Beta-Thalssemia-Mod.pdf

 

Bahrain Medical Bulletin, Vol. 32, No. 2, June 2010

Beta Thalassemia Frequency in Bahrain: A Ten Year Study

 

 

Shaikha Salim Al-Arrayed, MB,ChB, DHCG, PhD*

Background: Sickle-cell disease and Thalassanemia syndromes impose a significant economic burden on many countries. Their chronic nature makes them one of the leading causes of morbidity and mortality in those countries1.

Objective: The aim of this study is to estimate the frequency of beta thalassemia among the students in Bahrain from 1999 to 2008.

Setting: Bahraini Secondary Schools, genetic department and laboratory at Salmaniya medical complex.

Design: Prospective study.

Method: The students in the 11th grade (2nd Secondary class) were screened. Data were collected during the annual student screening program. Informed consents were obtained from the parents.

The blood samples were collected for hemoglobin electrophoresis using HPLC instrument.

Result: Sixty thousand students were screened from 1999 to 2008. The mean prevalence of beta thalassemia trait and major were 2097 (3.5%) and 19 (0.032%) respectively.

Conclusion: The frequency of beta thalassemia in Bahrain was found to be low to moderate compared with other Gulf countries such as UAE, Qatar and Kuwait. Sickle cell disease (SCD) is more common than beta thalassemia in Bahrain. Preventive measures remain the best ways for lowering the incidence of these diseases.

 
     
 

Archive

Title Date Visits

 Levels of pain control

28-09-2011 272

 Public Awareness of Glucose-6- Phosphate Dehydrogenase ( G6PD) Dificiency

11-08-2011 271

 fact about alpha thalassemia

10-08-2011 288

 Prevalence of Abnormal Hemoglobins among Students in Bahrain: A Ten-Year Study

09-03-2011 123

 Beta Thalassemia Frequency in Bahrain: A Ten Year Study

27-09-2010 119

 Public awareness of sickle cell disease in Bahrain

23-09-2010 109

 Premarital genetic counselling A new law in the kingdom of bahrain

23-09-2010 104

 links of several reserch published on Bahrain Medical Bulletin Journal

31-08-2010 110

 The risks and benefits of long-term use of hydroxyurea in sickle cell anemia: A 17.5 year follow-up.

22-06-2010 107

 Frequency of G6PD Deficiency among Bahraini students: A Ten Years Study

01-03-2010 104

الصفحات :1-2-3

الارشيف

العنوان التاريخ الزيارات
 

Public Awareness of Beta Thalassemia in Bahrain

05-04-2012 102
 

THE CHANGING PROFILE OF CONSANGUINITY

01-02-2012 107
 

Levels of pain control

28-09-2011 105
 

The Campaign to control genetic blood diseases in Bahrain.

09-03-2011 116
 

Prevalence of Abnormal Hemoglobins among Students in Bahrain: A Ten-Year Study

09-03-2011 108
 

Beta Thalassemia Frequency in Bahrain: A Ten Year Study

27-09-2010 106
 

Premarital genetic counselling A new law in the kingdom of bahrain

09-03-2011 114
 

Public awareness of sickle cell disease in bahrain

09-03-2011 174
 

روابط لأبحاث مختلفة من مجلة البحرين الطبية

07-07-2010 110
 

Frequency of G6PD Deficiency among Bahraini students: A Ten Years Study

07-07-2010 107

الصفحات :1-2-3-4