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- Check5 days agoChange DetectedThe page's revision label in the footer changed from v3.5.4 to v3.5.5, indicating a minor system/template update. No study data or public information about the trial was modified.SummaryDifference0.0%

- Check12 days agoNo Change Detected
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- Check26 days agoChange DetectedRevision tag updated from v3.5.3 to v3.5.4. This indicates a newer version of the page's versioning metadata, with no changes to the displayed study information.SummaryDifference0.0%

- Check40 days agoChange DetectedRevision tag on the page updated from v3.5.2 to v3.5.3, indicating a software version update. This likely reflects a backend or UI improvement without changing the study text or data presented.SummaryDifference0.0%

- Check55 days agoChange DetectedRevision: v3.5.2 was added; Revision: v3.5.0 was removed.SummaryDifference0.0%

- Check69 days agoChange DetectedAdded a related topic 'Severe myoclonic epilepsy in infancy' and a 'Genetic and Rare Diseases Information Center' resources section.SummaryDifference0.1%

- Check76 days agoChange DetectedDravet syndrome is no longer listed on the page and the Genetics and Rare Diseases Information Center resource link has been removed, decreasing disease-specific context and external reference options for users.SummaryDifference0.1%

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