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- CheckyesterdayChange DetectedRevision: v3.5.4 was added to the page, replacing v3.5.3 to indicate a maintenance/version update. This change does not modify study content or other user-facing information.SummaryDifference0.1%

- Check8 days agoChange DetectedFooter revision tag updated from v3.5.2 to v3.5.3, representing a minor software update. It is a metadata change that does not alter the study details displayed.SummaryDifference0.1%

- Check22 days agoNo Change Detected
- Check29 days agoChange DetectedFooter revision updated from v3.5.0 to v3.5.2.SummaryDifference0.1%

- Check44 days agoChange DetectedAdded a related topic Severe myoclonic epilepsy in infancy and a resources entry for the Genetic and Rare Diseases Information Center.SummaryDifference0.2%

- Check51 days agoChange DetectedThe study description no longer lists Dravet syndrome. The Genetic and Rare Diseases Information Center resource reference has been removed.SummaryDifference0.2%

- Check58 days agoChange DetectedSite revision updated from v3.4.3 to v3.5.0.SummaryDifference0.1%

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