Sökning: "synnedsättning"
Visar resultat 1 - 5 av 16 avhandlingar innehållade ordet synnedsättning.
1. A Sound Approach Toward a Mobility Aid for Blind and Low-Vision Individuals
Sammanfattning : Reduced independent mobility of blind and low-vision individuals (BLVIs) cause considerable societal cost, burden on relatives, and reduced quality of life for the individuals, including increased anxiety, depression symptoms, need of assistance, risk of falls, and mortality. Despite the numerous electronic travel aids proposed since at least the 1940’s, along with ever-advancing technology, the mobility issues persist. LÄS MER
2. Att lära, att göra, att klara : Förmedling av datortekniska hjälpmedel till barn med synnedsättning. Från förskrivning till vardaglig användning i skola och hem
Sammanfattning : Förmåga att använda informations- och kommunikationsteknik framhålls numeraofta som en förutsättning för delaktighet på lika villkor i samhällslivet. Näraförknippat med detta är de insatser som görs för att överbrygga digitala klyftor isamhället. LÄS MER
3. Förskjutna horisonter. Livsförändring och lärande i samband med synnedsättning eller blindhet
Sammanfattning : This study is an investigation of life-worlds of severely visually impaired and blind adults. The aim is to understand changes which people undergo when struck by severe visual impairment or blindness, focusing on how people learn to handle their changed life situation. LÄS MER
4. Clinical expressions of juvenile hereditary retinal degenerations and macular dystrophies: Electrophysiological and genetic studies
Sammanfattning : Hereditary retinal degenerations are the most frequent reason for severe visual handicap among young people in Scandinavia today. In the six papers included in this thesis the phenotypic expressions, with emphasis on the electrophysiological findings, of five different juvenile hereditary retinal degenerations are described. LÄS MER
5. Phenotypes and genotypes in families with hereditary tapetoretinal degenerations
Sammanfattning : The purpose of the study was to characterise the phenotype with emphasis on electroretinography in four different types of hereditary retinal degeneration and to correlate it to a genotype when possible. Two methods were used: full-field electroretinography for objective assessment of retinal function and mutation screening of blood samples for detection of gene alterations. LÄS MER