Article
The GAIRS Checklist: a useful global assessment tool in patients with Rett syndrome.
Orphanet journal of rare diseases - 5 Mar 2022
Fabio Rosa Angela, Semino Martina, Giannatiempo Samantha
Abstract excerpt
BACKGROUND: Rett Syndrome is a severe, neurodevelopmental disorder mainly caused by mutations in the MECP2 gene, affecting around 1 in 10,000 female births. Severe physical, language, and social impairments impose a wide range of limitations in the assessment of the abilities of Rett patients. This study proposes an analysis and first validation of a Global Assessment and Intervention in Rett syndrome (GAIRS)...
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