منابع مشابه
Unilateral retinitis pigmentosa sine pigmento.
A patient presented with unilateral findings of night blindness shown by impaired rod function and dark adaptation, constricted visual fields with good central acuity, a barely recordable electro-retinographic b-wave, and a unilaterally impaired electro-oculogram. There were none of the pigmentary changes usually associated with retinitis pigmentosa. The unaffected right eye was normal in all r...
متن کاملDorzolamide in management of cystoid macular edema in a patient with retinitis pigmentosa sine pigmento
Jelena KARADŽIĆ Clinical Centre of Serbia, Clinic for Eye Diseases, Pasterova 2, Belgrade, Serbia [email protected] SUMMARY Introduction Retinitis pigmentosa (RP) is a group of inherited retinal dystrophies caused by mutations in various genes. The disease leads to progressive photoreceptors loss (rods predominantly) and retinal pigment epithelium alteration. RP can lead to blindness in the ad...
متن کاملRetinitis pigmentosa sine pigmenti. Debut with macular oedema.
CASE REPORT A 25-year-old woman, with metamorphopsia in her left eye of one year onset. The examination revealed a bilateral cystoid macular oedema (CME) and vascular attenuation. We describe the diagnostic tests, as well as differential diagnosis and treatment response with carbonic anhydrase inhibitors. DISCUSSION The retinitis pigmentosa sine pigment is a subtype of atypical retinitis pigm...
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 ...
متن کاملRetinitis pigmentosa
Retinitis pigmentosa (RP) is an inherited retinal dystrophy caused by the loss of photoreceptors and characterized by retinal pigment deposits visible on fundus examination. Prevalence of non syndromic RP is approximately 1/4,000. The most common form of RP is a rod-cone dystrophy, in which the first symptom is night blindness, followed by the progressive loss in the peripheral visual field in ...
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ژورنال
عنوان ژورنال: Proceedings of the Royal Society of Medicine
سال: 1937
ISSN: 0035-9157
DOI: 10.1177/003591573703000414