منابع مشابه
A Case of Coats’-Like Retinitis Pigmentosa
We present a case of Coats’-like retinitis pigmentosa in a 22-year-old female patient. Both eyes showed the typical funduscopic features of retinitis pigmentosa, and the right eye showed scar formation due to exudative retinal detachment in the temporal peripheral retina with dilatation of the retinal vessels. Fluorescein angiography did not show dye leakage at the scar lesion or the dilated re...
متن کامل[Unilateral retinitis pigmentosa or pseudoretinitis pigmentosa? Case report].
Unilateral retinitis pigmentosa is a rare disease characterized by loss of photoreceptors and retinal pigment deposition without affecting the contralateral eye. Although described more than one hundred years its existence is still questioned. This article reports a case of a patient with abnormalities suggestive of unilateral retinitis pigmentosa. The clinical and complementary examinations ar...
متن کاملA Family of Congenital Hepatic Fibrosis and Atypical Retinitis Pigmentosa
Congenital hepatic fibrosis is a rare cause of portal hypertension and esophageal varices in children. We report cases of siblings with biopsy proven congenital hepatic fibrosis and with atypical retinitis pigmentosa. They presented with repeated episodes of jaundice along with progressive decrease of vision in night. They had hepatosplenomegaly and portal hypertension with esophageal varices. ...
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: The American Journal of the Medical Sciences
سال: 1872
ISSN: 0002-9629
DOI: 10.1097/00000441-187207000-00011