Search for dissertations about: "Rett syndrome RTT"
Showing result 1 - 5 of 6 swedish dissertations containing the words Rett syndrome RTT.
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1. Rett syndrome, motor development, mobility and orthostatic reactions : loss of function, difficulties and possibilities
Abstract : Rett syndrome (RTT) is a rare, severe neurodevelopmental disorder, which partly develops in a predictable way, and influences many bodily functions. Regression, i.e. loss of earlier achieved abilities, is one of the clinical criteria for RTT. READ MORE
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2. Genetic studies of children with mental retardation
Abstract : Mental retardation (MR) is characterised by significant limitations in intellectual function and adaptive behaviour. It is estimated that MR affects up to 3% of the population in Europe. Patients with MR are an aetiologically heterogeneous group. Approximately 25-35% of the patients have a genetic diagnosis. READ MORE
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3. Time for Activities for Girls and Women with Rett Syndrome
Abstract : Irrespective of the great individual variation, people diagnosed with RTT largely rely on support from others to be able to do and participate in activities throughout their lives. This thesis focuses on which activities are done and liked/disliked by girls and women with RTT in Sweden. READ MORE
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4. Health-enhancing participation in girls and women with Rett syndrome - a balancing act
Abstract : Rett syndrome (RTT) is a rare neurodevelopmental disorder usually affecting females. It is associated with multiple disabilities including intellectual disability leading to a high level of dependency in all aspects of daily living including participation in physical activities. READ MORE
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5. Downstream effects of master regulators in two brain diseases
Abstract : In paper one, we investigated how the pharmacological activation and inhibition of the glucocorticoid system affects lifespan and symptoms in a mouse model for RTT. We performed a long-term drug treatment study with the GR activator corticosterone and the GR inhibitor RU486 under which we measured the lifespan and onset of RTT-like symptoms of male Mecp2-null and female Mecp2 heterozygous mice in comparison to untreated mutant and to treated and untreated wild-type animals. READ MORE