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Showing results for "preterm birth lungs"
Rett syndrome (RTT) is a rare neurodevelopmental disorder mainly affecting females and is caused by a mutation in the MECP2 gene. Recent research identified the domains of quality of life (QOL) important for children with RTT but there has been no investigation of domains important for adults. This qualitative study explored QOL in adults with RTT and compared domains with those previously identified for children.
Individuals with Rett syndrome (RTT) experience impaired gross motor skills, limiting their capacity to engage in physical activities and participation in activities. There is limited evidence of the effectiveness of supported physical activity interventions. This study aims to evaluate the effects of a telehealth-delivered physical activity programme on physical activity, sedentary behaviour and quality of life in RTT.
To review the effectiveness of oral health education and oral health promotion interventions for children and adolescents with intellectual and developmental disabilities (IDD), in ensuring optimal gingival health, caries experience and oral health-related quality of life, compared to no interventions or alternative interventions.
Prader-Willi syndrome (PWS) is a rare genetic condition with multi-system involvement
Review of the available dental literature on assessment and management of the oral manifestations of Rett syndrome
Quality of life of young people with Down syndrome was most negatively associated with burden of medical conditions, but also with lack of friendships
People with intellectual disability were more likely to experience potentially preventable conditions at the end of their lives
This study aimed to validate measures of sedentary time in individuals with Rett syndrome.
Review of the clinical and biological progress over 50 years in Rett Syndrome
Mothers of children with autism without ID had increased risk of cancer, which may relate to common genetic pathways