]> http://JNNPR.edwiserinternational.com/rss-feed.php Edwiser-Journal-of-Neurology-Neurosurgery-Psychiatry-Research: VOLUME Volume 7 ISSUE Issue 1, Jan-June 2026 en-us editor@edwiserinternational.com editor@edwiserinternational.com editor@edwiserinternational.com http://JNNPR.edwiserinternational.com/rss-feed.php http://JNNPR.edwiserinternational.com/img/logo1.png 360 109 13-May-2026 http://JNNPR.edwiserinternational.com/admin/uploads/v51GD6.pdf Sanjiv-Chamraj-and-Sharan-Srinivasan {http://www.edwiserinternational.com/contact-us.php} Medical Science,Clinical Science {} 06-Aug-2026 http://JNNPR.edwiserinternational.com/admin/uploads/fFzWGj.pdf Chamraj-S-Srinivasan-S- {http://www.edwiserinternational.com/contact-us.php} Medical Science,Clinical Science {Glp.Gln2255Arg detected in the CACNA1G gene on chromosomal position chr17:50626381:A>G that can leads to a change in amino acid from Glutamine to Arginine at codon 2255. The whole exome sequencing of patients mothers sisters son identified the autosomal dominant heterozygous triple nucleotide CAG repeat number of approximately 54 4 in the PPP2R2B gene that can leads to pathogenic SCA12 expression. These findings emphasize the fact that SCA42 could masquerade as SCA12 in clinical presentation could be due to pathogenic SCA12 expression in the same family member. In conclusion, we reported the first novel case from Indian subcontinent that the heterozygous missense variant c.6764A>Glp.Gln2255Arg detected in the CACNA1G gene on chromosomal position chr17:50626381:A>G in 65-year-old male patient could masquerade as SCA12 in clinical presentation with clinical features of predominant hand tremors followed by ataxic gait.]]>}