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This study explored facilitators and barriers to "uptime" (non-sedentary) activities in Danish girls and women with Rett syndrome
High levels of sedentary time and low daily step counts in a Danish population of females with Rett syndrome
Gastrostomy placement was associated with improvement in BMI in females with Rett syndrome, but its long-term impact on individuals and their families is unclear
We aimed to: (1) describe the patterns of sedentary time and daily steps and (2) identify the association of individual and environmental characteristitics.
You can't stop loving them: the gift of a grandchild can sometimes be painful, writes Wendy Macklin.
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.
The U-PART intervention was found to be feasible and effective in the short term in girls and women with Rett Syndrome
Our findings suggest that some opportunities do exist for clinicians to help optimise parental well-being
This study investigated the capacity of three accelerometer-type devices to measure walking activity in Rett syndrome
We describe change in gross motor function over 3 to 4 years for 70 subjects participating in the Australian Rett Syndrome Database