Sökning: "vision impairment"
Visar resultat 11 - 15 av 52 avhandlingar innehållade orden vision impairment.
11. On vision in old age. A longitudinal study of subjects 70 to 97 years old
Sammanfattning : Aims. The main purpose of this study was to investigate different aspects of vision and visual function in old people, like change in vision and visual ability, to study the natural course of eye diseases, assess needs of visual intervention, investigate risk factors for ocular disorders late in life, and also to investigate coexistence between visual and hearing impairments. LÄS MER
12. Aspects on Function in Age-Related Macular Degeneration
Sammanfattning : Age-related macular degeneration (AMD) is one of the leading causes of severe visual loss among persons ≥ 60 years. AMD can be categorized in one of three stages: early, intermediate, or late. In early AMD visual symptoms are inconspicuous whereas, in the late stage, severe loss of vision is common. Late AMD has dry and wet forms. LÄS MER
13. Visual, musculoskeletal, and balance symptoms in people with visual impairments
Sammanfattning : Background: Worldwide, about 300 million people have some kind of visual impairment (VI). Most people with VI are in the older age range, as visual deficits increase with age. It is not unusual that people with VI suffer both from neck pain or scapular area symptoms and reduced balance, which they consider to be symptoms of old age. LÄS MER
14. From Cradle to Grave : Empirical Essays on Health and Economic Outcomes
Sammanfattning : This thesis contains four independent research papers, which investigate the causal relations between several aspects of health and economic outcomes at different stages of the life course. The first paper investigates the causal effects of maternal deprivation and maltreatment during various periods of childhood on adolescent health and human capital. LÄS MER
15. Congenital and Childhood Myotonic Dystrophy type 1 - the impact on central nervous system, visual and motor function
Sammanfattning : Background and aims: Myotonic dystrophy type 1 (DM1) is an autosomal dominant multisystemic disorder, caused by an expanded CTG repeat on chromosome 19. The disorder can present both in children and adults. LÄS MER