Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/114015
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dc.contributor.authorJavadiyan, S.en
dc.contributor.authorLucas, S.en
dc.contributor.authorWangmo, D.en
dc.contributor.authorNgy, M.en
dc.contributor.authorEdussuriya, K.en
dc.contributor.authorCraig, J.en
dc.contributor.authorRudkin, A.en
dc.contributor.authorCasson, R.en
dc.contributor.authorSelva, D.en
dc.contributor.authorSharma, S.en
dc.contributor.authorLower, K.en
dc.contributor.authorMeucke, J.en
dc.contributor.authorBurdon, K.en
dc.date.issued2018en
dc.identifier.citationMolecular Genetics and Genomic Medicine, 2018; 6(4):555-564en
dc.identifier.issn2324-9269en
dc.identifier.issn2324-9269en
dc.identifier.urihttp://hdl.handle.net/2440/114015-
dc.description.abstractBackground: Pediatric cataract is an important cause of blindness and visual impairment in children. A large proportion of pediatric cataracts are inherited, and many genes have been described for this heterogeneous Mendelian disease. Surveys of schools for the blind in Bhutan, Cambodia, and Sri Lanka have identified many children with this condition and we aimed to identify the genetic causes of inherited cataract in these populations. Methods: We screened, in parallel, 51 causative genes for inherited cataracts in 33 probands by Ampliseq enrichment and sequencing on an Ion Torrent PGM. Rare novel protein coding variants were assessed for segregation in family members, where possible, by Sanger sequencing. Results: We identified 24 rare (frequency <1% in public databases) or novel protein coding variants in 12 probands and confirmed segregation of variants with disease in the extended family where possible. Of these, six are predicted to be the cause of disease in the patient, with four other variants also highly likely to be pathogenic. Conclusion: This study found that 20%–30% of patients in these countries have a mutation in a known cataract causing gene, which is considerably lower than the 60%–70% reported in Caucasian cohorts. This suggests that additional cataract genes remain to be discovered in this cohort of Asian pediatric cataract patients.en
dc.description.statementofresponsibilityShari Javadiyan, Sionne E. M. Lucas, Dechen Wangmo, Meng Ngy, Kapila Edussuriya, Jamie E. Craig, Adam Rudkin, Robert Casson, Dinesh Selva, Shiwani Sharma, Karen M. Lower, James Meucke, Kathryn P. Burdonen
dc.language.isoenen
dc.publisherWileyen
dc.rights© 2018 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.en
dc.subjectcongenital cataract; inherited eye disease; mutation screening; next-generation sequencingen
dc.titleIdentification of novel mutations causing pediatric cataract in Bhutan, Cambodia, and Sri Lankaen
dc.typeJournal articleen
dc.identifier.rmid0030086979en
dc.identifier.doi10.1002/mgg3.406en
dc.identifier.pubid419872-
pubs.library.collectionOpthalmology & Visual Sciences publicationsen
pubs.library.teamDS03en
pubs.verification-statusVerifieden
pubs.publication-statusPublisheden
dc.identifier.orcidCasson, R. [0000-0003-2822-4076]en
dc.identifier.orcidSelva, D. [0000-0002-2169-5417]en
Appears in Collections:Opthalmology & Visual Sciences publications

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