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综述:了解印度查谟和克什米尔等资源匮乏地区的罕见遗传病

Review: Understanding Rare Genetic Diseases in Low Resource Regions Like Jammu and Kashmir - India.

作者信息

Angural Arshia, Spolia Akshi, Mahajan Ankit, Verma Vijeshwar, Sharma Ankush, Kumar Parvinder, Dhar Manoj Kumar, Pandita Kamal Kishore, Rai Ekta, Sharma Swarkar

机构信息

Human Genetics Research Group, School of Biotechnology, Shri Mata Vaishno Devi University, Katra, India.

Bioinformatics Infrastructure Facility, School of Biotechnology, Shri Mata Vaishno Devi University, Katra, India.

出版信息

Front Genet. 2020 Apr 30;11:415. doi: 10.3389/fgene.2020.00415. eCollection 2020.

Abstract

Rare diseases (RDs) are the clinical conditions affecting a few percentage of individuals in a general population compared to other diseases. Limited clinical information and a lack of reliable epidemiological data make their timely diagnosis and therapeutic management difficult. Emerging Next-Generation DNA Sequencing technologies have enhanced our horizons on patho-physiological understanding of many of the RDs and ushered us into an era of diagnostic and therapeutic research related to this ignored health challenge. Unfortunately, relevant research is meager in developing countries which lack a reliable estimate of the exact burden of most of the RDs. India is to be considered as the "Pandora's Box of genetic disorders." Owing to its huge population heterogeneity and high inbreeding or endogamy rates, a higher burden of rare recessive genetic diseases is expected and supported by the literature findings that endogamy is highly detrimental to health as it enhances the degree of homozygosity of recessive alleles in the general population. The population of a low resource region Jammu and Kashmir (J&K) - India, is highly inbred. Some of its population groups variably practice consanguinity. In context with the region's typical geographical topography, highly inbred population structure and unique but heterogeneous gene pool, a huge burden of known and uncharacterized genetic disorders is expected. Unfortunately, many suspected cases of genetic disorders remain undiagnosed or misdiagnosed due to lack of appropriate clinical as well as diagnostic resources in the region, causing patients to face a huge psycho-socio-economic crisis and many a time suffer life-long with their ailment. In this review, the major challenges associated with RDs are highlighted in general and an account on the methods that can be adopted for conducting fruitful molecular genetic studies in genetically vulnerable and low resource regions is also provided, with an example of a region like J&K - India.

摘要

与其他疾病相比,罕见病(RDs)是影响普通人群中少数个体的临床病症。有限的临床信息和可靠流行病学数据的缺乏使得对其进行及时诊断和治疗管理变得困难。新兴的下一代DNA测序技术拓宽了我们对许多罕见病病理生理理解的视野,并引领我们进入了与这一被忽视的健康挑战相关的诊断和治疗研究时代。不幸的是,在发展中国家,相关研究匮乏,对大多数罕见病的确切负担缺乏可靠估计。印度被视为“遗传疾病的潘多拉魔盒”。由于其庞大的人口异质性以及高近亲结婚或族内通婚率,预计罕见隐性遗传病的负担会更高,文献研究结果也支持这一点,即族内通婚对健康极为不利,因为它会增加普通人群中隐性等位基因的纯合度。印度资源匮乏地区查谟和克什米尔(J&K)的人口高度近亲结婚。其一些人群不同程度地存在近亲关系。鉴于该地区典型的地理地形、高度近亲结婚的人口结构以及独特但异质的基因库,预计会有大量已知和未知的遗传疾病负担。不幸的是,由于该地区缺乏适当的临床和诊断资源,许多疑似遗传疾病病例仍未得到诊断或被误诊,导致患者面临巨大的心理 - 社会 - 经济危机,并且很多时候要终身忍受病痛折磨。在本综述中,总体上突出了与罕见病相关的主要挑战,并以印度查谟和克什米尔这样的地区为例,说明了在遗传易感性高和资源匮乏地区进行富有成效的分子遗传学研究可采用的方法。

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