Frequencies of the MEFV Gene Mutations in Azerbaijan.

IF 0.5 4区 医学 Q4 GENETICS & HEREDITY
Balkan Journal of Medical Genetics Pub Date : 2022-06-05 eCollection Date: 2021-11-01 DOI:10.2478/bjmg-2021-0017
L S Huseynova, S N Mammadova, Kaa Aliyeva
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引用次数: 3

Abstract

The MEFV (familial Mediterranean fever gene) researches were performed in the population of the Republic of Azerbaijan in 2016-2021. Seven mutations of the MEFV gene were identified in heterozygous, homozygous and compound homozygous conditions: R761H, M694I, M694V, V726A, R202Q, M680I and E148Q. The E148Q and R202Q mutations were discovered in exon 2 and R761H M694I, M694V, V726A, M680I were found in exon 10 in the population of the Republic of Azerbaijan. The highest gene frequency of the MEFV gene examined in 42 patients was 42.85% in the M694V mutations. The second highest frequency was the R761H and the third most frequent mutation was V726A. According to world literature, five mutations, M694V, V726A, M694I, R202Q, M680I and E148Q, constitute 75.0% of all mutations found today. In our studies, these five mutations belong to the same group, and makes up 57.6% of the total mutations found. In order to prevent hereditary disease such as the familial Mediterranean fever (FMF) in the population of the Republic of Azerbaijan, it is planned to carry out prenatal diagnosis (PND) of the at-risk families.

Abstract Image

Abstract Image

阿塞拜疆MEFV基因突变的频率。
2016-2021年在阿塞拜疆共和国人群中进行了家族性地中海热基因(MEFV)研究。在杂合子、纯合子和复合纯合子条件下鉴定出7个MEFV基因突变:R761H、M694I、M694V、V726A、R202Q、M680I和E148Q。E148Q和R202Q突变在阿塞拜疆共和国人群的外显子2和R761H中发现。M694I, M694V, V726A, M680I在外显子10中发现。42例MEFV基因在M694V突变中最高基因频率为42.85%。第二高的突变是R761H,第三高的突变是V726A。根据世界文献,M694V、V726A、M694I、R202Q、M680I和E148Q这五种突变构成了今天发现的所有突变的75.0%。在我们的研究中,这五种突变属于同一组,占发现突变总数的57.6%。为了预防阿塞拜疆共和国人口中的家族性地中海热(FMF)等遗传性疾病,计划对高危家庭进行产前诊断。
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来源期刊
CiteScore
1.00
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: Balkan Journal of Medical Genetics is a journal in the English language for publication of articles involving all branches of medical genetics: human cytogenetics, molecular genetics, clinical genetics, immunogenetics, oncogenetics, pharmacogenetics, population genetics, genetic screening and diagnosis of monogenic and polygenic diseases, prenatal and preimplantation genetic diagnosis, genetic counselling, advances in treatment and prevention.
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