Genetic counseling in the context of Bangladesh: current scenario, challenges, and a framework for genetic service implementation

Author:

Hosen Mohammad JakirORCID,Anwar SaeedORCID,Taslem Mourosi JarinORCID,Chakraborty SouravORCID,Miah Md. FaruqueORCID,Vanakker Olivier M.ORCID

Abstract

AbstractWith the advancements in genetics and genomics in the twenty-first century, genetic services have become an integral part of medical practices in high-income and upper-middle-income countries. However, people living in low and lower-middle-income countries (LICs and LIMCs), including Bangladesh, are rather underprivileged in receiving genetic services. Consequently, genetic disorders are emerging as a significant public health concern in these countries. Lack of expertise, high expense, the dearth of epidemiological data, insufficiently updated medical education system, poor infrastructure, and the absence of comprehensive health policies are the main factors causing people living in these countries not having access to genetic services. In this article, the authors took benefit from their professional experience of practicing medical genetics in the area and reviewed existing literature to provide their opinions. Particularly, it reviews the current knowledge of genetic disorders' burden and their causative factors in Bangladesh. It focuses on why providing genetic services is challenging in the context of the country's cultural and religious sentiment. Finally, it proposes a physician-academician collaborative framework within the existing facility that aims to tackle the challenges. Such a framework could also be useful for other LICs and LMICs to address the challenges associated with providing genetic services.

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Genetics(clinical),General Medicine

Reference159 articles.

1. McKusick VA. Mendelian inheritance in man and its online version. OMIM Am J Hum Genet. 2007;80:588–604.

2. Samuels E. Saturation of the human phenome. Curr Genomics. 2010;11:482–99.

3. Black N, Martineau F, Manacorda T. Diagnostic odyssey for rare diseases:exploration of potential indicators [Internet]. London; 2015. https://piru.ac.uk/assets/files/RarediseasesFinalreport.pdf.

4. Baynam GS, Groft S, van der Westhuizen FH, Gassman SD, du Plessis K, Coles EP, et al. A call for global action for rare diseases in Africa. Nat Genet. 2020;52:21–6.

5. Genetic Alliance. Diagnosis of a genetic disease. In: Understanding genetics: a District of Columbia guide for patients and health professionals. Washington, DC: Genetic Alliance; 2010. p. 81.

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3