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Nat Genet ; 11(1): 27-32, 1995 Sep.
Article in English | MEDLINE | ID: mdl-7550309

ABSTRACT

Sorsby's fundus dystrophy (SFD) is an autosomal dominant retinal degeneration caused by mutations in the tissue inhibitor of metalloproteinases-3 (TIMP3) gene. Mechanisms of the visual loss in SFD, however, remain unknown. In a SFD family with a novel TIMP3 point mutation, we tested a hypothesis that their night blindness is due to a chronic deprivation of vitamin A at the level of the photoreceptors caused by a thickened membrane barrier between the photoreceptor layer and its blood supply. Vitamin A at 50,000 IU/d was administered orally. Within a week, the night blindness disappeared in patients at early stages of disease. Nutritional night blindness is thus part of the pathophysiology of this genetic disease and vitamin A supplementation can lead to dramatic restoration of photoreceptor function.


Subject(s)
Bruch Membrane/pathology , Eye Proteins/genetics , Fundus Oculi , Night Blindness/drug therapy , Proteins/genetics , Retinal Degeneration/complications , Retinal Rod Photoreceptor Cells/blood supply , Vitamin A/therapeutic use , Adult , Bruch Membrane/drug effects , Bruch Membrane/metabolism , DNA Mutational Analysis , Diffusion , Female , Humans , Male , Middle Aged , Night Blindness/etiology , Night Blindness/metabolism , Night Blindness/pathology , Pedigree , Point Mutation , Polymorphism, Single-Stranded Conformational , Retinal Degeneration/genetics , Retinal Degeneration/metabolism , Retinal Degeneration/pathology , Scotoma/drug therapy , Scotoma/etiology , Tissue Inhibitor of Metalloproteinase-3 , Vitamin A/administration & dosage , Vitamin A/pharmacokinetics
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