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Last Updated: 8 August 2024

Rett Syndrome

Rett Syndrome is a rare genetic neurological disorder affecting mainly girls, characterised by normal early growth followed by loss of motor skills and speech. Caused by mutations in the MECP2 gene, Rett Syndrome leads to severe cognitive and physical impairments, often requiring lifelong care. It typically manifests between 6-18 months of age.

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