非洲癫痫遗传学:挑战和未来展望。

Guida Landouré, Youssoufa Maiga, Oumar Samassékou, Karamoko Nimaga, Mahamadou Traoré, Kenneth H Fischbeck
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引用次数: 0

摘要

尽管非洲人口具有多样性,但对癫痫的遗传研究,特别是在撒哈拉以南非洲,一直有限。近年来,随着发展中国家传染病的减少,重点已更多地转向非传染性疾病。与其他大陆相比,非洲的癫痫患病率较高。虽然这归因于传染病的高发病率,但遗传因素也不应被忽视。非洲的遗传性癫痫研究可以很好地受益于遗传分析成本的降低,并有助于进一步了解非洲这些疾病的范围。非洲研究机构与发达国家研究机构之间日益加强的合作提供了一个独特的机会,可以促进非洲的研究,提高我们对人类疾病的全球了解,从而导致开发更好的治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Epilepsy genetics in Africa: challenges and future perspectives.

Despite the diversity of the African population, genetic studies, of epilepsy in particular, have been limited, especially in sub-Saharan Africa. In recent years, with the regression of infectious diseases in developing countries, the focus has shifted more towards non communicable disorders. The prevalence of epilepsy in Africa is higher compared to other continents. Although this has been attributed to the high rate of infectious diseases, genetic contributions should not be ignored. Research in genetic epilepsy in Africa could well benefit from the decreasing cost of genetic analysis, and could contribute to further our knowledge on the spectrum of these diseases in Africa. The growing collaboration between African research institutions and those of developed countries offers a unique opportunity to boost research in Africa and improve our global understanding of human disease, thus leading to the development of better therapeutic approaches.

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