Literature DB >> 20001628

Steps toward the prevention of hemoglobinopathies in the kingdom of Saudi Arabia.

Mohammad Al-Shahrani1.   

Abstract

Saudi Arabia is known to have high prevalence of hereditary blood disorder similar to neighboring Mediterranean countries, in particular sickle-cell disease and thalassemia. With increasing number of affected individual (Saadallah AA, Rashed MS. J Inherit Metab Dis. 2007;30:482-489), the Ministry of Health (MOH) had implemented a mandatory premarital testing for hemoglobinopathies (sickle-cell disease and thalassemia). Since November 2003, all Saudi couples planning for marriage are required to perform the test (Alhamdan NA, Almazrou YY, Alswaidi FM, Coudhry AJ. Genet Med. 2007;9(6):372-377). Besides its preventive efforts, the MOH had also increased its efforts to improve the health care given to affected hereditary blood disease patients. To that effect, a plan to increase the number of specialized hereditary blood disease centers in different regions is existing. In addition, a Consultation Board, Hereditary Blood Disease Advisory Committee, was formed in January 2008. This committee, under the directorate of MOH, took the responsibility of laying down the foundation for internationally high standard of medical care given in treatment center dealing with patients with hereditary blood disorders. In this report, we will shed some light on such accomplishment.

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Year:  2009        PMID: 20001628     DOI: 10.3109/03630260903346437

Source DB:  PubMed          Journal:  Hemoglobin        ISSN: 0363-0269            Impact factor:   0.849


  5 in total

1.  Effects of -3.7α Deletion and Sickle-Cell Trait on Ventilatory and Hemodynamic Responses to Maximum Exercise in Young Saudi Females.

Authors:  Lubna Ibrahim Al Asoom; Marwah Mansour Al Makhaita; Nazish Rafique; Dina Tariq Al Afandi; Waad Mohammed Al Otaibi; Hind Saleh Alsuwat; Mousa A Alaithan; Sayed AbdulAzeez; J Francis Borgio
Journal:  J Blood Med       Date:  2020-10-20

2.  Six-year outcome of the national premarital screening and genetic counseling program for sickle cell disease and β-thalassemia in Saudi Arabia.

Authors:  Ziad Ahmed Memish; Mohammad Y Saeedi
Journal:  Ann Saudi Med       Date:  2011 May-Jun       Impact factor: 1.526

Review 3.  Sickle cell disease in Middle East Arab countries.

Authors:  Mohsen A F El-Hazmi; Ali M Al-Hazmi; Arjumand S Warsy
Journal:  Indian J Med Res       Date:  2011-11       Impact factor: 2.375

4.  Quantifying the Levels of Knowledge, Attitude, and Practice Associated with Sickle Cell Disease and Premarital Genetic Counseling in 350 Saudi Adults.

Authors:  Heba M Al-Qattan; Dana F Amlih; Fatima S Sirajuddin; Dalal I Alhuzaimi; Mai S Alageel; Reema M Bin Tuwaim; Farjah H Al Qahtani
Journal:  Adv Hematol       Date:  2019-05-02

Review 5.  Molecular nature of alpha-globin genes in the Saudi population.

Authors:  J Francis Borgio
Journal:  Saudi Med J       Date:  2015-11       Impact factor: 1.484

  5 in total

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