Pain in Rett syndrome: a pilot study and a single case study on the assessment of pain and the construction of a suitable measuring scale
Rett Syndrome (RTT) 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...
Source: Orphanet Journal of Rare Diseases - Category: Internal Medicine Authors: Rosa Angela Fabio, Liliana Chiarini and Virginia Canegallo Tags: Research Source Type: research
More News: Brain | Genetics | Internal Medicine | Neurology | Pain | Rare Diseases | Rett Syndrome | Study