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Spinocerebellar ataxia type 6 in eastern India: Some new observations
Introduction: Spinocerebellar ataxias (SCAs) are hereditary, autosomal dominant progressive neurodegenerative disorders showing clinical and genetic heterogeneity. They are usually manifested clinically in the third to fifth decade of life although there is a wide variability in the age of onset. Mo...
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Published in: | Annals of the Indian Academy of Neurology 2016-07, Vol.19 (3), p.360-366 |
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creator | Bhattacharyya, Kalyan Pulai, Debabrata Guin, Deb Ganguly, Goutam Joardar, Anindita Roy, Sarnava Rai, Saurabh Biswas, Atanu Pandit, Alok Roy, Arijit Senapati, Asit |
description | Introduction: Spinocerebellar ataxias (SCAs) are hereditary, autosomal dominant progressive neurodegenerative disorders showing clinical and genetic heterogeneity. They are usually manifested clinically in the third to fifth decade of life although there is a wide variability in the age of onset. More than 36 different types of SCAs have been reported so far and about half of them are caused by pathological expansion of the trinucleotide, Cytosine Alanine Guanine (CAG) repeat. The global prevalence of SCA is 0.3-2 per 100,000 population, SCA3 being the commonest variety worldwide, accounting for 20-50 per cent of all cases, though SCA 2 is generally considered as the commonest one in India. However, SCA6 has not been addressed adequately from India though it is common in the eastern Asian countries like, Japan, Korea and Thailand. Objective: The present study was undertaken to identify the prevalence of SCA6 in the city of Kolkata and the eastern part of India. Materials and Methods: 83 consecutive patients were recruited for the study of possible SCAs and their clinical features and genotype were investigated. Results: 6 of the 83 subjects turned out positive for SCA6, constituting therefore, 13.33% of the patient pool. Discussion: SCA6 is prevalent in the eastern part of India, though not as frequent as the other common varieties. Conclusions: Further community based studies are required in order to understand the magnitude of SCA6 in the eastern part, as well as in other regions of India. |
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They are usually manifested clinically in the third to fifth decade of life although there is a wide variability in the age of onset. More than 36 different types of SCAs have been reported so far and about half of them are caused by pathological expansion of the trinucleotide, Cytosine Alanine Guanine (CAG) repeat. The global prevalence of SCA is 0.3-2 per 100,000 population, SCA3 being the commonest variety worldwide, accounting for 20-50 per cent of all cases, though SCA 2 is generally considered as the commonest one in India. However, SCA6 has not been addressed adequately from India though it is common in the eastern Asian countries like, Japan, Korea and Thailand. Objective: The present study was undertaken to identify the prevalence of SCA6 in the city of Kolkata and the eastern part of India. Materials and Methods: 83 consecutive patients were recruited for the study of possible SCAs and their clinical features and genotype were investigated. Results: 6 of the 83 subjects turned out positive for SCA6, constituting therefore, 13.33% of the patient pool. Discussion: SCA6 is prevalent in the eastern part of India, though not as frequent as the other common varieties. Conclusions: Further community based studies are required in order to understand the magnitude of SCA6 in the eastern part, as well as in other regions of India.</description><identifier>ISSN: 0972-2327</identifier><identifier>EISSN: 1998-3549</identifier><identifier>DOI: 10.4103/0972-2327.186823</identifier><identifier>PMID: 27570389</identifier><language>eng</language><publisher>India: Wolters Kluwer - Medknow Publications</publisher><subject>Ataxia ; Care and treatment ; Deoxyribonucleic acid ; Diagnosis ; DNA ; Eastern India ; Family medical history ; Genes ; Metabolism ; Mutation ; Original ; Phenols ; SCA6 ; Spinocerebellar ataxia ; Studies</subject><ispartof>Annals of the Indian Academy of Neurology, 2016-07, Vol.19 (3), p.360-366</ispartof><rights>COPYRIGHT 2016 Medknow Publications and Media Pvt. Ltd.</rights><rights>Copyright Medknow Publications & Media Pvt Ltd Jul-Sep 2016</rights><rights>Copyright: © Annals of Indian Academy of Neurology 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c687r-b271026dc4e098ffbb20fac90bd2ae9b664436cb657c8997f01184d7fd74e8063</citedby><cites>FETCH-LOGICAL-c687r-b271026dc4e098ffbb20fac90bd2ae9b664436cb657c8997f01184d7fd74e8063</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4980960/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1837052409?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27458,27924,27925,37012,37013,44590,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27570389$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bhattacharyya, Kalyan</creatorcontrib><creatorcontrib>Pulai, Debabrata</creatorcontrib><creatorcontrib>Guin, Deb</creatorcontrib><creatorcontrib>Ganguly, Goutam</creatorcontrib><creatorcontrib>Joardar, Anindita</creatorcontrib><creatorcontrib>Roy, Sarnava</creatorcontrib><creatorcontrib>Rai, Saurabh</creatorcontrib><creatorcontrib>Biswas, Atanu</creatorcontrib><creatorcontrib>Pandit, Alok</creatorcontrib><creatorcontrib>Roy, Arijit</creatorcontrib><creatorcontrib>Senapati, Asit</creatorcontrib><title>Spinocerebellar ataxia type 6 in eastern India: Some new observations</title><title>Annals of the Indian Academy of Neurology</title><addtitle>Ann Indian Acad Neurol</addtitle><description>Introduction: Spinocerebellar ataxias (SCAs) are hereditary, autosomal dominant progressive neurodegenerative disorders showing clinical and genetic heterogeneity. They are usually manifested clinically in the third to fifth decade of life although there is a wide variability in the age of onset. More than 36 different types of SCAs have been reported so far and about half of them are caused by pathological expansion of the trinucleotide, Cytosine Alanine Guanine (CAG) repeat. The global prevalence of SCA is 0.3-2 per 100,000 population, SCA3 being the commonest variety worldwide, accounting for 20-50 per cent of all cases, though SCA 2 is generally considered as the commonest one in India. However, SCA6 has not been addressed adequately from India though it is common in the eastern Asian countries like, Japan, Korea and Thailand. Objective: The present study was undertaken to identify the prevalence of SCA6 in the city of Kolkata and the eastern part of India. Materials and Methods: 83 consecutive patients were recruited for the study of possible SCAs and their clinical features and genotype were investigated. Results: 6 of the 83 subjects turned out positive for SCA6, constituting therefore, 13.33% of the patient pool. Discussion: SCA6 is prevalent in the eastern part of India, though not as frequent as the other common varieties. Conclusions: Further community based studies are required in order to understand the magnitude of SCA6 in the eastern part, as well as in other regions of India.</description><subject>Ataxia</subject><subject>Care and treatment</subject><subject>Deoxyribonucleic acid</subject><subject>Diagnosis</subject><subject>DNA</subject><subject>Eastern India</subject><subject>Family medical history</subject><subject>Genes</subject><subject>Metabolism</subject><subject>Mutation</subject><subject>Original</subject><subject>Phenols</subject><subject>SCA6</subject><subject>Spinocerebellar ataxia</subject><subject>Studies</subject><issn>0972-2327</issn><issn>1998-3549</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqNkk1vEzEQhlcIREPhzgmtxIXLBn-tPzgglapApEocCmfL6x0Hpxs72JuG_nsc0kYJygH5YMl-5tHM6K2q1xhNGUb0PVKCNIQSMcWSS0KfVBOslGxoy9TTarL_Pqte5LxAqOWM8ufVGRGtQFSqSXV1s_IhWkjQwTCYVJvR_PamHu9XUPPahxpMHiGFehZ6bz7UN3EJdYBNHbsM6c6MPob8snrmzJDh1cN9Xv34fPX98mtz_e3L7PLiurFcitR0RGBEeG8ZICWd6zqCnLEKdT0xoDrOWenPdrwVViolHMJYsl64XjCQiNPzarbz9tEs9Cr5pUn3Ohqv_z7ENNcmjd4OoJFj0jIrJLOMWeo6QnsnGMXCgVWyL66PO9dq3S2htxDGZIYj6fFP8D_1PN5ppiRSHBXBuwdBir_WkEe99NlutxggrrPGUmLRUibUf6C4pbwlfIu-_QddxHUKZauFogK1hKEDam7KrD64WFq0W6m-YK2iSpTBC9WcoOYQoMwTAzhfno_46Qm-nB6W3p4sQLsCm2LOCdx-fRjpbUL1NoJ6G0G9S2gpeXO49n3BYyQL8GkHbOJQgpdvh_UGki7sbYibI3FzINaUI_0YZvoHP3bzHQ</recordid><startdate>20160701</startdate><enddate>20160701</enddate><creator>Bhattacharyya, Kalyan</creator><creator>Pulai, Debabrata</creator><creator>Guin, Deb</creator><creator>Ganguly, Goutam</creator><creator>Joardar, Anindita</creator><creator>Roy, Sarnava</creator><creator>Rai, Saurabh</creator><creator>Biswas, Atanu</creator><creator>Pandit, Alok</creator><creator>Roy, Arijit</creator><creator>Senapati, Asit</creator><general>Wolters Kluwer - Medknow Publications</general><general>Medknow Publications and Media Pvt. 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They are usually manifested clinically in the third to fifth decade of life although there is a wide variability in the age of onset. More than 36 different types of SCAs have been reported so far and about half of them are caused by pathological expansion of the trinucleotide, Cytosine Alanine Guanine (CAG) repeat. The global prevalence of SCA is 0.3-2 per 100,000 population, SCA3 being the commonest variety worldwide, accounting for 20-50 per cent of all cases, though SCA 2 is generally considered as the commonest one in India. However, SCA6 has not been addressed adequately from India though it is common in the eastern Asian countries like, Japan, Korea and Thailand. Objective: The present study was undertaken to identify the prevalence of SCA6 in the city of Kolkata and the eastern part of India. Materials and Methods: 83 consecutive patients were recruited for the study of possible SCAs and their clinical features and genotype were investigated. Results: 6 of the 83 subjects turned out positive for SCA6, constituting therefore, 13.33% of the patient pool. Discussion: SCA6 is prevalent in the eastern part of India, though not as frequent as the other common varieties. Conclusions: Further community based studies are required in order to understand the magnitude of SCA6 in the eastern part, as well as in other regions of India.</abstract><cop>India</cop><pub>Wolters Kluwer - Medknow Publications</pub><pmid>27570389</pmid><doi>10.4103/0972-2327.186823</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Ataxia Care and treatment Deoxyribonucleic acid Diagnosis DNA Eastern India Family medical history Genes Metabolism Mutation Original Phenols SCA6 Spinocerebellar ataxia Studies |
title | Spinocerebellar ataxia type 6 in eastern India: Some new observations |
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