Literature DB >> 16113536

United Arab Emirates: communities and community genetics.

L I Al-Gazali1, R Alwash, Y M Abdulrazzaq.   

Abstract

The UAE society is cosmopolitan, but the indigenous inhabitants are traditional with puritanical values despite their exposure to other vastly different cultures and habits. Marriages between consanguineous couples are still the norm rather than the exception. As a result, there is a high frequency of genetic disorders, particularly autosomal recessive types. Despite the high frequency of genetic disorders like haemoglobinopathies and others characteristically found in this population, genetic services are inadequate. Screening for certain disorders like thalassaemia are not applied on a wide scale. Abortion is illegal, and therefore, prenatal diagnosis or preconception tests are not done. With the absence of a good national database, deficiency of genetic services and absence of preventative alternatives for carrier couples, genetic counsellors find it difficult to advice pragmatic solutions to issues relating to genetic diseases. This paper reviews common genetic problems in the UAE with special emphasis on available genetic services and support to families with children with inherited disorders. Existing barriers to the improvement of clinical services by prenatal counselling are also discussed.

Entities:  

Mesh:

Year:  2005        PMID: 16113536     DOI: 10.1159/000086764

Source DB:  PubMed          Journal:  Community Genet        ISSN: 1422-2795


  13 in total

Review 1.  Genetic disorders in the Arab world.

Authors:  Lihadh Al-Gazali; Hanan Hamamy; Shaikha Al-Arrayad
Journal:  BMJ       Date:  2006-10-21

2.  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

3.  Identification of mutations underlying 20 inborn errors of metabolism in the United Arab Emirates population.

Authors:  Imen Ben-Rebeh; Jozef L Hertecant; Fatma A Al-Jasmi; Hanan E Aburawi; Said A Al-Yahyaee; Lihadh Al-Gazali; Bassam R Ali
Journal:  Genet Test Mol Biomarkers       Date:  2011-11-22

Review 4.  Vitamin D in the Persian Gulf: integrative physiology and socioeconomic factors.

Authors:  Jessica Fields; Nishant J Trivedi; Edward Horton; Jeffrey I Mechanick
Journal:  Curr Osteoporos Rep       Date:  2011-12       Impact factor: 5.096

Review 5.  The future of cystic fibrosis care: a global perspective.

Authors:  Scott C Bell; Marcus A Mall; Hector Gutierrez; Milan Macek; Susan Madge; Jane C Davies; Pierre-Régis Burgel; Elizabeth Tullis; Claudio Castaños; Carlo Castellani; Catherine A Byrnes; Fiona Cathcart; Sanjay H Chotirmall; Rebecca Cosgriff; Irmgard Eichler; Isabelle Fajac; Christopher H Goss; Pavel Drevinek; Philip M Farrell; Anna M Gravelle; Trudy Havermans; Nicole Mayer-Hamblett; Nataliya Kashirskaya; Eitan Kerem; Joseph L Mathew; Edward F McKone; Lutz Naehrlich; Samya Z Nasr; Gabriela R Oates; Ciaran O'Neill; Ulrike Pypops; Karen S Raraigh; Steven M Rowe; Kevin W Southern; Sheila Sivam; Anne L Stephenson; Marco Zampoli; Felix Ratjen
Journal:  Lancet Respir Med       Date:  2019-09-27       Impact factor: 30.700

6.  Hurler disease (mucopolysaccharidosis type IH): clinical features and consanguinity in Tunisian population.

Authors:  Latifa Chkioua; Souhir Khedhiri; Hadhami Ben Turkia; Henda Chahed; Salima Ferchichi; Marie Françoise Ben Dridi; Sandrine Laradi; Abdelhedi Miled
Journal:  Diagn Pathol       Date:  2011-11-10       Impact factor: 2.644

7.  Thalassemia in the United Arab Emirates: Why it can be prevented but not eradicated.

Authors:  Sehjeong Kim; Abdessamad Tridane
Journal:  PLoS One       Date:  2017-01-30       Impact factor: 3.240

8.  Hemoglobin A2 Lowered by Iron Deficiency and α -Thalassemia: Should Screening Recommendation for β -Thalassemia Change?

Authors:  Srdjan Denic; Mukesh M Agarwal; Bayan Al Dabbagh; Awad El Essa; Mohamed Takala; Saad Showqi; Javed Yassin
Journal:  ISRN Hematol       Date:  2013-03-12

9.  Significantly elevated foetal haemoglobin levels in individuals with glucose 6-phosphate dehydrogenase disease and/or sickle cell trait: a cross-sectional study in Cape Coast, Ghana.

Authors:  Patrick Adu; Essel K M Bashirudeen; Florence Haruna; Edward Morkporkpor Adela; Richard K D Ephraim
Journal:  BMC Hematol       Date:  2017-09-25

10.  Consanguinity and major genetic disorders in Saudi children: a community-based cross-sectional study.

Authors:  Mohammad I El Mouzan; Abdullah A Al Salloum; Abdullah S Al Herbish; Mansour M Qurachi; Ahmad A Al Omar
Journal:  Ann Saudi Med       Date:  2008 May-Jun       Impact factor: 1.526

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