Cytogenetic Analysis of Down Syndrome

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dc.creatorKadakol, G S
dc.creatorBagoji, Ishwar
dc.creatorPatil, S V
dc.creatorBulagouda, R S
dc.date.accessioned2026-01-10T19:35:22Z
dc.date.available2026-01-10T19:35:22Z
dc.date.issued2019-01-27
dc.descriptionObjective: Down syndrome is a common genetic disease, diagnosed with congenital malformation/mental retardation. Down syndrome occurs in all races & economic levels. It is caused by third copy of chromosome 21, there are there forms of DS. Simple Trisomy 21, Translocation Trisomy and Mosaic Trisomy. The aim of the study is to know cause of Down syndrome. Chromosomal analysis was carried out by G banding technique. Materials and Methods: 1 ml of peripheral blood samples were collected in Out Patient Department of pediatrics and Cytogenetic analysis was performed. Results: out of 28, 3 female cases, 2 male cases were Down syndrome, All the 5 cases were free trisomy 21, which is common type of Down syndrome; we have not identified Robertsonian translocation and mosaic type of DS. Conclusion: The present analysis shows that genetic risk factors are responsible for the incidence of Down syndrome.en-US
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dc.identifierhttps://sumathipublications.com/index.php/ijcbr/article/view/259
dc.identifier10.31878/ijcbr.2018.51.10
dc.identifier.urihttps://repos.sumathipublications.com:8000/handle/123456789/304
dc.languageeng
dc.publisherSumathi Publicationsen-US
dc.relationhttps://sumathipublications.com/index.php/ijcbr/article/view/259/287
dc.relation.ispartofInternational Journal of Clinical and Biomedical Researchen-US
dc.relation.ispartofseriesVolume 5, Issue 1en-US
dc.rightsCopyright (c) 2019 G S Kadakol, Ishwar Bagoji, S V Patil, R S Bulagoudaen-US
dc.sourceInternational Journal of Clinical and Biomedical Research; Volume 5, Issue 1; Jan 2019.; 37-40en-US
dc.source2395-0471
dc.source2521-0394
dc.titleCytogenetic Analysis of Down Syndromeen-US
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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International Journal of Clinical and Biomedical Research (IJCBR)