AI Article Synopsis

  • Rare diseases (RDs) affect a small percentage of the population and face challenges like limited clinical information and unreliable epidemiological data, making diagnosis and treatment difficult.
  • * Emerging DNA sequencing technologies are improving our understanding of RDs, but research in developing countries remains minimal, especially in India, which has a high incidence of genetic disorders due to population diversity and endogamy.
  • * In regions like Jammu and Kashmir, high inbreeding rates and a lack of diagnostic resources lead to many individuals with genetic disorders remaining undiagnosed, resulting in significant socio-economic burdens for patients and their families.*

Article 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7203485PMC
http://dx.doi.org/10.3389/fgene.2020.00415DOI Listing

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