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

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-Gener...

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Autores principales: Angural, Arshia, Spolia, Akshi, Mahajan, Ankit, Verma, Vijeshwar, Sharma, Ankush, Kumar, Parvinder, Dhar, Manoj Kumar, Pandita, Kamal Kishore, Rai, Ekta, Sharma, Swarkar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7203485/
https://www.ncbi.nlm.nih.gov/pubmed/32425985
http://dx.doi.org/10.3389/fgene.2020.00415
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author Angural, Arshia
Spolia, Akshi
Mahajan, Ankit
Verma, Vijeshwar
Sharma, Ankush
Kumar, Parvinder
Dhar, Manoj Kumar
Pandita, Kamal Kishore
Rai, Ekta
Sharma, Swarkar
author_facet Angural, Arshia
Spolia, Akshi
Mahajan, Ankit
Verma, Vijeshwar
Sharma, Ankush
Kumar, Parvinder
Dhar, Manoj Kumar
Pandita, Kamal Kishore
Rai, Ekta
Sharma, Swarkar
author_sort Angural, Arshia
collection PubMed
description 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.
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spelling pubmed-72034852020-05-18 Review: Understanding Rare Genetic Diseases in Low Resource Regions Like Jammu and Kashmir – India Angural, Arshia Spolia, Akshi Mahajan, Ankit Verma, Vijeshwar Sharma, Ankush Kumar, Parvinder Dhar, Manoj Kumar Pandita, Kamal Kishore Rai, Ekta Sharma, Swarkar Front Genet Genetics 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. Frontiers Media S.A. 2020-04-30 /pmc/articles/PMC7203485/ /pubmed/32425985 http://dx.doi.org/10.3389/fgene.2020.00415 Text en Copyright © 2020 Angural, Spolia, Mahajan, Verma, Sharma, Kumar, Dhar, Pandita, Rai and Sharma. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Angural, Arshia
Spolia, Akshi
Mahajan, Ankit
Verma, Vijeshwar
Sharma, Ankush
Kumar, Parvinder
Dhar, Manoj Kumar
Pandita, Kamal Kishore
Rai, Ekta
Sharma, Swarkar
Review: Understanding Rare Genetic Diseases in Low Resource Regions Like Jammu and Kashmir – India
title Review: Understanding Rare Genetic Diseases in Low Resource Regions Like Jammu and Kashmir – India
title_full Review: Understanding Rare Genetic Diseases in Low Resource Regions Like Jammu and Kashmir – India
title_fullStr Review: Understanding Rare Genetic Diseases in Low Resource Regions Like Jammu and Kashmir – India
title_full_unstemmed Review: Understanding Rare Genetic Diseases in Low Resource Regions Like Jammu and Kashmir – India
title_short Review: Understanding Rare Genetic Diseases in Low Resource Regions Like Jammu and Kashmir – India
title_sort review: understanding rare genetic diseases in low resource regions like jammu and kashmir – india
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7203485/
https://www.ncbi.nlm.nih.gov/pubmed/32425985
http://dx.doi.org/10.3389/fgene.2020.00415
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