Sökning: "myotonic dystrophy"
Visar resultat 1 - 5 av 14 avhandlingar innehållade orden myotonic dystrophy.
1. Myotonic dystrophy type 1. Cognition, personality and emotion
Sammanfattning : kommer senare.... LÄS MER
2. On oral health in children and adults with myotonic dystrophy
Sammanfattning : Background: Myotonic Dystrophy type 1 (DM1) is a hereditary neuromuscular multisystem disease with varying clinical expressions and severity. The prevalence worldwide is 5-20/100 000. It is characterized by progressive muscular waste and myotonia. Facial weakness is one of the earliest and most constant features. LÄS MER
3. Muscle strength and motor function in neuromuscular disorders. A clinical study of children and adolescents with spinal muscular atrophy, myotonic dystrophy, Duchenne muscular dystrophy and amyoplasia
Sammanfattning : Aim: The aims of this study were to investigate muscle strength and motor function in children and adolescents with four neuromuscular disorders; 1) spinal muscular atrophy (SMA), 2) myotonic dystrophy (DM), 3) Duchenne muscular dystrophy (DMD and 4) the amyoplasia form of arthrogryposis multiplex congenita. Further: 1) to analyze compensatory maneuvers due to muscle weakness in individuals with SMA, 2) to correlate motor function in individuals with DM with the size of the mutation, 3) to evaluate the long-term side effects and effects on muscle strength, motor function, vital capacity and development of scoliosis in boys with DMD treated with low-dose prednisone, and 4) to investigate how muscle strength and joint contractures affect motor function in individuals with amyoplasia and to relate current status to joint position at birth. LÄS MER
4. Personality and facial emotion recognition ability in myotonic dystrophy type 1
Sammanfattning : .... LÄS MER
5. Living with muscular dystrophy : Illness experience, activities of daily living, coping, quality of life and rehabilitation
Sammanfattning : The overall aim was to study and gain knowledge about what it means to live with muscular dystrophy and to study rehabilitation from the patient's perspective, among adults with muscular dystrophy in three Swedish counties: Örebro, Östergötland and Norrbotten. The thesis comprises two qualitative and three quantitative studies. LÄS MER