منابع مشابه
Retinitis pigmentosa and Gaucher's disease.
Past History.-He had measles as a child, and had occasionally suffered from malaria, the last attack occurring in 1950; he stated that it took him much longer than the average person to recover from an attack, which usually lasted about a fortnight. As a baby of. about one year he had developed recurrent attacks of pyrexia. His spleen was found to be enlarged, and steadily increased in size. Th...
متن کاملRetinitis pigmentosa and Coats's disease.
The association of two rare ocular conditions of unknown aetiology presents the clinician with an opportunity to study interrelating factors. The association of retinitis pigmentosa with Coats's disease has been previously reported in three patients (Zamorani, I956; Morgan and Crawford, I968), in all of whom bilateral involvement occurred with severe visual loss. The present case which has been...
متن کاملRetinitis Pigmentosa: Disease Mechanisms, Diagnosis, and Therapies
1Department of Life Sciences, Glasgow Caledonian University, Glasgow G4 0BA, UK 2School of Ophthalmology & Optometry, The Eye Hospital, Wenzhou Medical University, Wenzhou, Zhejiang 325027, China 3Department of Ophthalmology, College of Medicine, University of Florida, Gainesville, FL 32610, USA 4Sichuan Provincial Key Laboratory for Disease Gene Study, Hospital of University of Electronic Scie...
متن کاملRetinitis Pigmentosa: Genes and Disease Mechanisms
Retinitis pigmentosa (RP) is a group of inherited disorders affecting 1 in 3000-7000 people and characterized by abnormalities of the photoreceptors (rods and cones) or the retinal pigment epithelium of the retina which lead to progressive visual loss. RP can be inherited in an autosomal dominant, autosomal recessive or X-linked manner. While usually limited to the eye, RP may also occur as par...
متن کاملRetinitis pigmentosa.
Hereditary degenerations of the human retina are genetically heterogeneous, with well over 100 genes implicated so far. This Seminar focuses on the subset of diseases called retinitis pigmentosa, in which patients typically lose night vision in adolescence, side vision in young adulthood, and central vision in later life because of progressive loss of rod and cone photoreceptor cells. Measures ...
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ژورنال
عنوان ژورنال: British Journal of Ophthalmology
سال: 1976
ISSN: 0007-1161
DOI: 10.1136/bjo.60.11.775