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- ChecktodayChange DetectedUpdate to the page revision label from v3.5.4 to v3.5.5, indicating a small update to the page's documentation or content. This appears to be a minor patch rather than a substantive change to the page's core information.SummaryDifference0.1%

- Check8 days agoNo Change Detected
- Check15 days agoNo Change Detected
- Check22 days agoChange 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%

- Check29 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%

- Check50 days agoChange DetectedFooter revision updated from v3.5.0 to v3.5.2.SummaryDifference0.1%

- Check65 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%

- Check72 days agoChange DetectedThe study description no longer lists Dravet syndrome. The Genetic and Rare Diseases Information Center resource reference has been removed.SummaryDifference0.2%

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