Sökning: "Bothnia Dystrophy"
Hittade 4 avhandlingar innehållade orden Bothnia Dystrophy.
1. Bothnia dystrophy, a clinical, genetical and electrophysiological study
Sammanfattning : A high frequency of retinitis pigmentosa (RP) is found in Northern Sweden. In an inventory of autosomal recessive RP patients in Västerbotten County, a great number of cases with a unique phenotype was noticed, denoted Bothnia Dystrophy (BD). LÄS MER
2. Evaluation of the visual pathway with ERG, mfERG and mfVEP in inherited eye disorders
Sammanfattning : This thesis will describe the clinical phenotypes, with emphasis on electrophysiology, in patients with different hereditary eye diseases and to further evaluate and modify the mfVEP technique for clinical use. Bothnia Dystrophy is a tapetoretinal disorder with a mutation in the RLBP1 gene. LÄS MER
3. Genetic mapping of retinal degenerations in Northern Sweden
Sammanfattning : Inherited retinal degenerations are a group of disorders characterised by great genetic heterogeneity. Clinically, they can be divided into two large groups of diseases, those associated with night blindness, e.g. retinitis pigmentosa (RP), and those with macular malfunction, e. LÄS MER
4. Underlying genetic mechanisms of hereditary dystrophies in retina and cornea
Sammanfattning : Inherited retinal and corneal dystrophies represent a group of disorders with great genetic heterogeneity. Over 250 genes are associated with retinal diseases and 16 genes are causative of corneal dystrophies. LÄS MER