Loading…

Diagnostic outcome of pro bono neurogenetic diagnostic service in Sri Lanka: A wealth creation

The inherited disease community in Sri Lanka has been widely neglected. This article aimed to present accumulated knowledge in establishing a pro bono cost-effective national, island-wide, free-of-charge molecular diagnostic service, suggesting a model for other developing countries. The project pro...

Full description

Saved in:
Bibliographic Details
Published in:European journal of human genetics : EJHG 2024-01, Vol.32 (10), p.1299-1306
Main Authors: Gonawala, Lakmal, Wijekoon, Nalaka, Attanayake, Darshika, Ratnayake, Pyara, Sirisena, Darshana, Gunasekara, Harsha, Dissanayake, Athula, Keshavaraj, Ajantha, Mohan, Chandra, Steinbusch, Harry W. M., Hoffman, Eric P., Dalal, Ashwin, de Silva, K. Ranil D.
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites cdi_FETCH-LOGICAL-c426t-2d0d1ce675c33f8d42f9ce8074dd14205f7b4ce4a945db9b822c76f3978451c3
container_end_page 1306
container_issue 10
container_start_page 1299
container_title European journal of human genetics : EJHG
container_volume 32
creator Gonawala, Lakmal
Wijekoon, Nalaka
Attanayake, Darshika
Ratnayake, Pyara
Sirisena, Darshana
Gunasekara, Harsha
Dissanayake, Athula
Keshavaraj, Ajantha
Mohan, Chandra
Steinbusch, Harry W. M.
Hoffman, Eric P.
Dalal, Ashwin
de Silva, K. Ranil D.
description The inherited disease community in Sri Lanka has been widely neglected. This article aimed to present accumulated knowledge in establishing a pro bono cost-effective national, island-wide, free-of-charge molecular diagnostic service, suggesting a model for other developing countries. The project provided 637 molecular diagnostic tests and reports free of charge to a nation with limited resources. We pioneered the implementation of mobile clinics and home visits, where the research team acted as barefoot doctors with the concept of the doctor and the researcher at the patient’s doorstep. Establishing pro bono, cost-effective molecular diagnostics is feasible in developing countries with limited resources and state funding through the effort of dedicated postgraduate students. This service could provide an accurate molecular diagnosis of Duchenne muscular dystrophy, Huntington’s disease, Spinocerebellar ataxia, and Spinal muscular atrophy, a diagnostic yield of 54% (343/637), of which 43% (147/343) of the patients identified as amenable for available gene therapies. Initiated human resource development by double doctoral degree opportunities with international collaborations. Established a neurobiobank and a national registry in Sri Lanka, a rich and unique repository, wealth creation for translational collaborative research and sharing of information in neurological diseases, as well as a lodestar for aspiring initiatives from other developing countries.
doi_str_mv 10.1038/s41431-023-01525-3
format article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_11500083</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3119818775</sourcerecordid><originalsourceid>FETCH-LOGICAL-c426t-2d0d1ce675c33f8d42f9ce8074dd14205f7b4ce4a945db9b822c76f3978451c3</originalsourceid><addsrcrecordid>eNp9kc1u1DAUhS1ERUvhBVggS2y6CfX1T-ywQVX5qzQSC7rGcpybqUvGHuykiLfHw5S2sGBlS-fz8b36CHkB7DUwYU6LBCmgYVw0DBRXjXhEjkDqtlFSmMf1zsA00oA4JE9LuWashhqekENhuBLaiCPy9V1w65jKHDxNy-zTBmka6TYn2qeYaMQlpzVG3AHDPVsw3wSPNET6JQe6cvGbe0PP6A9003xFfUY3hxSfkYPRTQWf357H5PLD-8vzT83q88eL87NV4yVv54YPbACPrVZeiNEMko-dR8O0HAaQnKlR99KjdJ1UQ9_1hnOv21F02kgFXhyTt_va7dJvcPAY5-wmu81h4_JPm1ywfycxXNl1urEAijFmRG04uW3I6fuCZbabUDxOk4uYlmJ5B9q0DEBX9NU_6HVacqzrWQHQGTBaq0rxPeVzKiXjeDcNMLvTZ_f6bNVnf-uzuylePtzj7skfXxUQe6DUKK4x3__9n9pfPu6mLw</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3119818775</pqid></control><display><type>article</type><title>Diagnostic outcome of pro bono neurogenetic diagnostic service in Sri Lanka: A wealth creation</title><source>Springer Link</source><creator>Gonawala, Lakmal ; Wijekoon, Nalaka ; Attanayake, Darshika ; Ratnayake, Pyara ; Sirisena, Darshana ; Gunasekara, Harsha ; Dissanayake, Athula ; Keshavaraj, Ajantha ; Mohan, Chandra ; Steinbusch, Harry W. M. ; Hoffman, Eric P. ; Dalal, Ashwin ; de Silva, K. Ranil D.</creator><creatorcontrib>Gonawala, Lakmal ; Wijekoon, Nalaka ; Attanayake, Darshika ; Ratnayake, Pyara ; Sirisena, Darshana ; Gunasekara, Harsha ; Dissanayake, Athula ; Keshavaraj, Ajantha ; Mohan, Chandra ; Steinbusch, Harry W. M. ; Hoffman, Eric P. ; Dalal, Ashwin ; de Silva, K. Ranil D.</creatorcontrib><description>The inherited disease community in Sri Lanka has been widely neglected. This article aimed to present accumulated knowledge in establishing a pro bono cost-effective national, island-wide, free-of-charge molecular diagnostic service, suggesting a model for other developing countries. The project provided 637 molecular diagnostic tests and reports free of charge to a nation with limited resources. We pioneered the implementation of mobile clinics and home visits, where the research team acted as barefoot doctors with the concept of the doctor and the researcher at the patient’s doorstep. Establishing pro bono, cost-effective molecular diagnostics is feasible in developing countries with limited resources and state funding through the effort of dedicated postgraduate students. This service could provide an accurate molecular diagnosis of Duchenne muscular dystrophy, Huntington’s disease, Spinocerebellar ataxia, and Spinal muscular atrophy, a diagnostic yield of 54% (343/637), of which 43% (147/343) of the patients identified as amenable for available gene therapies. Initiated human resource development by double doctoral degree opportunities with international collaborations. Established a neurobiobank and a national registry in Sri Lanka, a rich and unique repository, wealth creation for translational collaborative research and sharing of information in neurological diseases, as well as a lodestar for aspiring initiatives from other developing countries.</description><identifier>ISSN: 1018-4813</identifier><identifier>ISSN: 1476-5438</identifier><identifier>EISSN: 1476-5438</identifier><identifier>DOI: 10.1038/s41431-023-01525-3</identifier><identifier>PMID: 38253783</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>38/22 ; 45/23 ; 45/29 ; 45/77 ; 631/208/2489/1512 ; 631/378/2583 ; Bioinformatics ; Biomedical and Life Sciences ; Biomedicine ; Cytogenetics ; Developing countries ; Duchenne's muscular dystrophy ; Gene Expression ; Gene therapy ; Hereditary diseases ; Hospitals ; Human Genetics ; LDCs ; Neurological diseases ; Neurosciences ; Resource development ; Specialty products ; Spinal muscular atrophy</subject><ispartof>European journal of human genetics : EJHG, 2024-01, Vol.32 (10), p.1299-1306</ispartof><rights>The Author(s) 2024</rights><rights>2024. The Author(s).</rights><rights>The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2024 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c426t-2d0d1ce675c33f8d42f9ce8074dd14205f7b4ce4a945db9b822c76f3978451c3</cites><orcidid>0000-0001-5929-745X ; 0000-0002-8738-9412</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38253783$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gonawala, Lakmal</creatorcontrib><creatorcontrib>Wijekoon, Nalaka</creatorcontrib><creatorcontrib>Attanayake, Darshika</creatorcontrib><creatorcontrib>Ratnayake, Pyara</creatorcontrib><creatorcontrib>Sirisena, Darshana</creatorcontrib><creatorcontrib>Gunasekara, Harsha</creatorcontrib><creatorcontrib>Dissanayake, Athula</creatorcontrib><creatorcontrib>Keshavaraj, Ajantha</creatorcontrib><creatorcontrib>Mohan, Chandra</creatorcontrib><creatorcontrib>Steinbusch, Harry W. M.</creatorcontrib><creatorcontrib>Hoffman, Eric P.</creatorcontrib><creatorcontrib>Dalal, Ashwin</creatorcontrib><creatorcontrib>de Silva, K. Ranil D.</creatorcontrib><title>Diagnostic outcome of pro bono neurogenetic diagnostic service in Sri Lanka: A wealth creation</title><title>European journal of human genetics : EJHG</title><addtitle>Eur J Hum Genet</addtitle><addtitle>Eur J Hum Genet</addtitle><description>The inherited disease community in Sri Lanka has been widely neglected. This article aimed to present accumulated knowledge in establishing a pro bono cost-effective national, island-wide, free-of-charge molecular diagnostic service, suggesting a model for other developing countries. The project provided 637 molecular diagnostic tests and reports free of charge to a nation with limited resources. We pioneered the implementation of mobile clinics and home visits, where the research team acted as barefoot doctors with the concept of the doctor and the researcher at the patient’s doorstep. Establishing pro bono, cost-effective molecular diagnostics is feasible in developing countries with limited resources and state funding through the effort of dedicated postgraduate students. This service could provide an accurate molecular diagnosis of Duchenne muscular dystrophy, Huntington’s disease, Spinocerebellar ataxia, and Spinal muscular atrophy, a diagnostic yield of 54% (343/637), of which 43% (147/343) of the patients identified as amenable for available gene therapies. Initiated human resource development by double doctoral degree opportunities with international collaborations. Established a neurobiobank and a national registry in Sri Lanka, a rich and unique repository, wealth creation for translational collaborative research and sharing of information in neurological diseases, as well as a lodestar for aspiring initiatives from other developing countries.</description><subject>38/22</subject><subject>45/23</subject><subject>45/29</subject><subject>45/77</subject><subject>631/208/2489/1512</subject><subject>631/378/2583</subject><subject>Bioinformatics</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cytogenetics</subject><subject>Developing countries</subject><subject>Duchenne's muscular dystrophy</subject><subject>Gene Expression</subject><subject>Gene therapy</subject><subject>Hereditary diseases</subject><subject>Hospitals</subject><subject>Human Genetics</subject><subject>LDCs</subject><subject>Neurological diseases</subject><subject>Neurosciences</subject><subject>Resource development</subject><subject>Specialty products</subject><subject>Spinal muscular atrophy</subject><issn>1018-4813</issn><issn>1476-5438</issn><issn>1476-5438</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp9kc1u1DAUhS1ERUvhBVggS2y6CfX1T-ywQVX5qzQSC7rGcpybqUvGHuykiLfHw5S2sGBlS-fz8b36CHkB7DUwYU6LBCmgYVw0DBRXjXhEjkDqtlFSmMf1zsA00oA4JE9LuWashhqekENhuBLaiCPy9V1w65jKHDxNy-zTBmka6TYn2qeYaMQlpzVG3AHDPVsw3wSPNET6JQe6cvGbe0PP6A9003xFfUY3hxSfkYPRTQWf357H5PLD-8vzT83q88eL87NV4yVv54YPbACPrVZeiNEMko-dR8O0HAaQnKlR99KjdJ1UQ9_1hnOv21F02kgFXhyTt_va7dJvcPAY5-wmu81h4_JPm1ywfycxXNl1urEAijFmRG04uW3I6fuCZbabUDxOk4uYlmJ5B9q0DEBX9NU_6HVacqzrWQHQGTBaq0rxPeVzKiXjeDcNMLvTZ_f6bNVnf-uzuylePtzj7skfXxUQe6DUKK4x3__9n9pfPu6mLw</recordid><startdate>20240123</startdate><enddate>20240123</enddate><creator>Gonawala, Lakmal</creator><creator>Wijekoon, Nalaka</creator><creator>Attanayake, Darshika</creator><creator>Ratnayake, Pyara</creator><creator>Sirisena, Darshana</creator><creator>Gunasekara, Harsha</creator><creator>Dissanayake, Athula</creator><creator>Keshavaraj, Ajantha</creator><creator>Mohan, Chandra</creator><creator>Steinbusch, Harry W. M.</creator><creator>Hoffman, Eric P.</creator><creator>Dalal, Ashwin</creator><creator>de Silva, K. Ranil D.</creator><general>Springer International Publishing</general><general>Nature Publishing Group</general><scope>C6C</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-5929-745X</orcidid><orcidid>https://orcid.org/0000-0002-8738-9412</orcidid></search><sort><creationdate>20240123</creationdate><title>Diagnostic outcome of pro bono neurogenetic diagnostic service in Sri Lanka: A wealth creation</title><author>Gonawala, Lakmal ; Wijekoon, Nalaka ; Attanayake, Darshika ; Ratnayake, Pyara ; Sirisena, Darshana ; Gunasekara, Harsha ; Dissanayake, Athula ; Keshavaraj, Ajantha ; Mohan, Chandra ; Steinbusch, Harry W. M. ; Hoffman, Eric P. ; Dalal, Ashwin ; de Silva, K. Ranil D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c426t-2d0d1ce675c33f8d42f9ce8074dd14205f7b4ce4a945db9b822c76f3978451c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>38/22</topic><topic>45/23</topic><topic>45/29</topic><topic>45/77</topic><topic>631/208/2489/1512</topic><topic>631/378/2583</topic><topic>Bioinformatics</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cytogenetics</topic><topic>Developing countries</topic><topic>Duchenne's muscular dystrophy</topic><topic>Gene Expression</topic><topic>Gene therapy</topic><topic>Hereditary diseases</topic><topic>Hospitals</topic><topic>Human Genetics</topic><topic>LDCs</topic><topic>Neurological diseases</topic><topic>Neurosciences</topic><topic>Resource development</topic><topic>Specialty products</topic><topic>Spinal muscular atrophy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gonawala, Lakmal</creatorcontrib><creatorcontrib>Wijekoon, Nalaka</creatorcontrib><creatorcontrib>Attanayake, Darshika</creatorcontrib><creatorcontrib>Ratnayake, Pyara</creatorcontrib><creatorcontrib>Sirisena, Darshana</creatorcontrib><creatorcontrib>Gunasekara, Harsha</creatorcontrib><creatorcontrib>Dissanayake, Athula</creatorcontrib><creatorcontrib>Keshavaraj, Ajantha</creatorcontrib><creatorcontrib>Mohan, Chandra</creatorcontrib><creatorcontrib>Steinbusch, Harry W. M.</creatorcontrib><creatorcontrib>Hoffman, Eric P.</creatorcontrib><creatorcontrib>Dalal, Ashwin</creatorcontrib><creatorcontrib>de Silva, K. Ranil D.</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>European journal of human genetics : EJHG</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gonawala, Lakmal</au><au>Wijekoon, Nalaka</au><au>Attanayake, Darshika</au><au>Ratnayake, Pyara</au><au>Sirisena, Darshana</au><au>Gunasekara, Harsha</au><au>Dissanayake, Athula</au><au>Keshavaraj, Ajantha</au><au>Mohan, Chandra</au><au>Steinbusch, Harry W. M.</au><au>Hoffman, Eric P.</au><au>Dalal, Ashwin</au><au>de Silva, K. Ranil D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Diagnostic outcome of pro bono neurogenetic diagnostic service in Sri Lanka: A wealth creation</atitle><jtitle>European journal of human genetics : EJHG</jtitle><stitle>Eur J Hum Genet</stitle><addtitle>Eur J Hum Genet</addtitle><date>2024-01-23</date><risdate>2024</risdate><volume>32</volume><issue>10</issue><spage>1299</spage><epage>1306</epage><pages>1299-1306</pages><issn>1018-4813</issn><issn>1476-5438</issn><eissn>1476-5438</eissn><abstract>The inherited disease community in Sri Lanka has been widely neglected. This article aimed to present accumulated knowledge in establishing a pro bono cost-effective national, island-wide, free-of-charge molecular diagnostic service, suggesting a model for other developing countries. The project provided 637 molecular diagnostic tests and reports free of charge to a nation with limited resources. We pioneered the implementation of mobile clinics and home visits, where the research team acted as barefoot doctors with the concept of the doctor and the researcher at the patient’s doorstep. Establishing pro bono, cost-effective molecular diagnostics is feasible in developing countries with limited resources and state funding through the effort of dedicated postgraduate students. This service could provide an accurate molecular diagnosis of Duchenne muscular dystrophy, Huntington’s disease, Spinocerebellar ataxia, and Spinal muscular atrophy, a diagnostic yield of 54% (343/637), of which 43% (147/343) of the patients identified as amenable for available gene therapies. Initiated human resource development by double doctoral degree opportunities with international collaborations. Established a neurobiobank and a national registry in Sri Lanka, a rich and unique repository, wealth creation for translational collaborative research and sharing of information in neurological diseases, as well as a lodestar for aspiring initiatives from other developing countries.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>38253783</pmid><doi>10.1038/s41431-023-01525-3</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0001-5929-745X</orcidid><orcidid>https://orcid.org/0000-0002-8738-9412</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1018-4813
ispartof European journal of human genetics : EJHG, 2024-01, Vol.32 (10), p.1299-1306
issn 1018-4813
1476-5438
1476-5438
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_11500083
source Springer Link
subjects 38/22
45/23
45/29
45/77
631/208/2489/1512
631/378/2583
Bioinformatics
Biomedical and Life Sciences
Biomedicine
Cytogenetics
Developing countries
Duchenne's muscular dystrophy
Gene Expression
Gene therapy
Hereditary diseases
Hospitals
Human Genetics
LDCs
Neurological diseases
Neurosciences
Resource development
Specialty products
Spinal muscular atrophy
title Diagnostic outcome of pro bono neurogenetic diagnostic service in Sri Lanka: A wealth creation
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-03T02%3A55%3A20IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Diagnostic%20outcome%20of%20pro%20bono%20neurogenetic%20diagnostic%20service%20in%20Sri%20Lanka:%20A%20wealth%20creation&rft.jtitle=European%20journal%20of%20human%20genetics%20:%20EJHG&rft.au=Gonawala,%20Lakmal&rft.date=2024-01-23&rft.volume=32&rft.issue=10&rft.spage=1299&rft.epage=1306&rft.pages=1299-1306&rft.issn=1018-4813&rft.eissn=1476-5438&rft_id=info:doi/10.1038/s41431-023-01525-3&rft_dat=%3Cproquest_pubme%3E3119818775%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c426t-2d0d1ce675c33f8d42f9ce8074dd14205f7b4ce4a945db9b822c76f3978451c3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=3119818775&rft_id=info:pmid/38253783&rfr_iscdi=true