Map of Autosomal Recessive Genetic Disorders in Saudi Arabia: Concepts and Future Directions

被引:65
作者
Al-Owain, Mohammed [1 ,2 ]
Al-Zaidan, Hamad [1 ,2 ]
Al-Hassnan, Zuhair [1 ,2 ]
机构
[1] King Faisal Specialist Hosp & Res Ctr, Dept Med Genet, Riyadh 11211, Saudi Arabia
[2] Alfaisal Univ, Coll Med, Riyadh, Saudi Arabia
关键词
autosomal recessive disorders; Saudi Arabia; consanguinity; tribe; founder mutations; allelic heterogeneity; autozygosity; exome sequencing; registry; prevention; TANDEM MASS-SPECTROMETRY; BASAL GANGLIA DISEASE; SICKLE-CELL-DISEASE; MOLECULAR CHARACTERIZATION; CONSANGUINEOUS FAMILIES; ALLELIC HETEROGENEITY; DIABETES-MELLITUS; ALPHA-THALASSEMIA; EASTERN PROVINCE; BETA-THALASSEMIA;
D O I
10.1002/ajmg.a.35551
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Saudi Arabia has a population of 27.1 million. Prevalence of many autosomal recessive disorders is higher than in other known populations. This is attributable to the high rate of consanguineous marriages (56%), the tribal structure, and large family size. Founder mutations have been recognized in many autosomal recessive disorders, many of which are overrepresented within certain tribes. On the other hand, allelic heterogeneity is also observed among common and rare autosomal recessive conditions. With the adoption of more advanced molecular techniques in the country in recent years in conjunction with international collaboration, the mapping of various autosomal recessive disorders has increased dramatically. Different genetic concepts pertinent to this highly inbred population are discussed here. Addressing such genetic disorders at the national level will become a cornerstone of strategic health care initiatives in the 21st century. Current efforts are hampered by many sociocultural and health care related factors. Education about genetic diseases, establishment of a "national registry" and mutational database, and enhanced healthcare access are crucial for success of any preventative campaign. (C) 2012 Wiley Periodicals, Inc.
引用
收藏
页码:2629 / 2640
页数:12
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