Literature DB >> 8131251

Hereditary disorders in the Eastern Mediterranean Region.

H Hamamy1, A Alwan.   

Abstract

Hereditary diseases and congenital malformations have been reported to affect 2-5% of all live births. Available evidence suggests that genetic disorders are equally important also in countries of the Eastern Mediterranean Region. Considerable achievements have been made over the last two decades in controlling communicable diseases in the region. Concurrently, there has been a mounting awareness of the increasing importance of hereditary disorders. Certain genetically determined diseases such as the haemoglobinopathies and enzymopathies are extremely common in the region and the need to initiate public health measures for their control is increasingly being recognized. The following factors may contribute to the elevated prevalence of genetically determined disorders: the high consanguinity rates; the high frequency of haemoglobinopathies and glucose-6-phosphate dehydrogenase deficiency; the trend of continuing to bear children up to menopause; the general lack of public awareness about genetic diseases; and the dearth of genetic services in the region. These and some other related issues are discussed in detail in this review article.

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Year:  1994        PMID: 8131251      PMCID: PMC2486500     

Source DB:  PubMed          Journal:  Bull World Health Organ        ISSN: 0042-9686            Impact factor:   9.408


  27 in total

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Authors:  A H Bittles; W M Mason; J Greene; N A Rao
Journal:  Science       Date:  1991-05-10       Impact factor: 47.728

2.  Inbreeding effects on reproductive outcome in a Sudanese population.

Authors:  N Saha; R E Hamad; S Mohamed
Journal:  Hum Hered       Date:  1990       Impact factor: 0.444

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Authors:  M Angastiniotis; S Kyriakidou; M Hadjiminas
Journal:  Birth Defects Orig Artic Ser       Date:  1988

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Authors:  R Cook; A Hanslip
Journal:  J Trop Pediatr Afr Child Health       Date:  1966-03

5.  Lethal malformations and perinatal mortality: a 10 year review with comparison of ethnic differences.

Authors:  I D Young; M Clarke
Journal:  Br Med J (Clin Res Ed)       Date:  1987-07-11

6.  Autosomal recessive "uncomplicated" profound childhood deafness in an Arabic family with high consanguinity.

Authors:  A Kabarity; S A Al-Awadi; T I Farag; G Mallalah
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

7.  Idiopathic recurrent spontaneous abortion. Evidence of a familial predisposition.

Authors:  O B Christiansen; O Mathiesen; J G Lauritsen; N Grunnet
Journal:  Acta Obstet Gynecol Scand       Date:  1990       Impact factor: 3.636

8.  Congenital abnormalities in newborns of consanguineous and nonconsanguineous parents.

Authors:  S Naderi
Journal:  Obstet Gynecol       Date:  1979-02       Impact factor: 7.661

9.  Consanguineous marriage and reproduction in Beirut, Lebanon.

Authors:  M Khlat
Journal:  Am J Hum Genet       Date:  1988-08       Impact factor: 11.025

10.  The frequency of glucose-6-phosphate dehydrogenase phenotypes and sickle cell gene in Al-Qassim.

Authors:  M A El-Hazmi; A S Warsy
Journal:  Ann Saudi Med       Date:  1992-09       Impact factor: 1.526

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  10 in total

1.  Consanguinity and advanced maternal age as risk factors for reproductive losses in Alexandria, Egypt.

Authors:  M M Mokhtar; M M Abdel-Fattah
Journal:  Eur J Epidemiol       Date:  2001       Impact factor: 8.082

2.  Causes of blindness at the "Wiyata Guna" School for the Blind, Indonesia.

Authors:  R Sitorus; M Preising; B Lorenz
Journal:  Br J Ophthalmol       Date:  2003-09       Impact factor: 4.638

3.  A review of the diverse genetic disorders in the Lebanese population: highlighting the urgency for community genetic services.

Authors:  Ghunwa Nakouzi; Khalil Kreidieh; Soha Yazbek
Journal:  J Community Genet       Date:  2014-09-27

4.  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

Review 5.  Transfusion in Haemoglobinopathies: Review and recommendations for local blood banks and transfusion services in Oman.

Authors:  Arwa Z Al-Riyami; Shahina Daar
Journal:  Sultan Qaboos Univ Med J       Date:  2018-04-04

6.  Next-generation community genetics for low- and middle-income countries.

Authors:  Stephen F Kingsmore; John D Lantos; Darrell L Dinwiddie; Neil A Miller; Sarah E Soden; Emily G Farrow; Carol J Saunders
Journal:  Genome Med       Date:  2012-03-29       Impact factor: 11.117

Review 7.  Genomics in Egypt: Current Status and Future Aspects.

Authors:  Eman Ahmed El-Attar; Rasha Mohamed Helmy Elkaffas; Sarah Ahmed Aglan; Iman S Naga; Amira Nabil; Hoda Y Abdallah
Journal:  Front Genet       Date:  2022-05-13       Impact factor: 4.772

8.  CTGA: the database for genetic disorders in Arab populations.

Authors:  Ghazi O Tadmouri; Mahmoud Taleb Al Ali; Sarah Al-Haj Ali; Najib Al Khaja
Journal:  Nucleic Acids Res       Date:  2006-01-01       Impact factor: 16.971

Review 9.  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

10.  Glucose-6-phosphate dehydrogenase deficiency among Yemeni children residing in malaria-endemic areas of Hodeidah governorate and evaluation of a rapid diagnostic test for its detection.

Authors:  Rashad Abdul-Ghani; Mohammed A K Mahdy; Reyadh Saif-Ali; Sameer A Alkubati; Abdulhabib R Alqubaty; Abdullah A Al-Mikhlafy; Samira M Al-Eryani; Abdusalam M Al-Mekhlafi; Ali Alhaj
Journal:  Malar J       Date:  2016-06-21       Impact factor: 2.979

  10 in total

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