United Arab Emirates: Communities and community genetics

被引:31
作者
Al-Gazali, LI
Alwash, R
Abdulrazzaq, YM
机构
[1] United Arab Emirates Univ, Fac Med & Hlth Sci, Dept Paediat, Al Ain, U Arab Emirates
[2] Minist Hlth, Dept Prevent Med, Al Ain, U Arab Emirates
关键词
United Arab Emirates; genetic disorders; genetic service; consanguinity;
D O I
10.1159/000086764
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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. Copyright (c) 2005 S. Karger AG, Basel.
引用
收藏
页码:186 / 196
页数:11
相关论文
共 46 条
  • [1] HB AL-AIN ABU-DHABI [ALPHA-18(A16)GLY-]ASP] - A NEW HEMOGLOBIN-VARIANT DISCOVERED IN AN EMIRATEE FAMILY
    ABBES, S
    MRAD, A
    FITZGERALD, PA
    DORMER, P
    BLOUQUIT, Y
    KISTER, J
    GALACTEROS, F
    WAJCMAN, H
    [J]. HEMOGLOBIN, 1992, 16 (05) : 355 - 362
  • [2] ABDULLA MM, 1978, UNITED ARAB EMIRATES, P221
  • [3] Abdulrazzaq YM, 1997, CLIN GENET, V51, P167
  • [4] Diversity in expression of glucose-6-phosphate dehydrogenase deficiency in females
    Abdulrazzaq, YM
    Micallef, R
    Qureshi, M
    Dawodu, A
    Ahmed, I
    Khidr, A
    Bastaki, SMA
    Al-Khayat, AI
    Bayoumi, RA
    [J]. CLINICAL GENETICS, 1999, 55 (01) : 13 - 19
  • [5] Pattern of central nervous system anomalies in a population with a high rate of consanguineous marriages
    Al-Gazali, L
    Sztriha, L
    Dawodu, A
    Bakir, M
    Varghese, M
    Varady, E
    Scorer, J
    Abdulrazzaq, Y
    Bener, A
    Padmanabhan, R
    [J]. CLINICAL GENETICS, 1999, 55 (02) : 95 - 102
  • [6] Attitudes toward genetic counseling in the United Arab Emirates
    Al-Gazali, LI
    [J]. COMMUNITY GENETICS, 2005, 8 (01) : 48 - 51
  • [7] Birth prevalence and pattern of osteochondrodysplasias in an inbred high risk population
    Al-Gazali, LI
    Bakir, M
    Hamid, Z
    Varady, E
    Varghes, M
    Haas, D
    Bener, A
    Padmanabhan, R
    Abdulrrazzzaq, YM
    Dawodu, AK
    [J]. BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY, 2003, 67 (02) : 125 - 132
  • [8] A genetic aetiological survey of severe childhood deafness in the United Arab Emirates
    Al-Gazali, LI
    [J]. JOURNAL OF TROPICAL PEDIATRICS, 1998, 44 (03) : 157 - 160
  • [9] Gerodermia osteodysplastica and wrinkly skin syndrome: Are they the same?
    Al-Gazali, LI
    Sztriha, L
    Skaff, F
    Haas, D
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 2001, 101 (03): : 213 - 220
  • [10] AlGazali LI, 1996, CLIN DYSMORPHOL, V5, P159