نتایج جستجو برای: congenital retinitis pigmentosa

تعداد نتایج: 128326  

Journal: :The British journal of ophthalmology 1976
D K Gahlot P K Khosla P D Makashir K Vasuki N Basu

Clinically and electrophysiologically confirmed cases of primary retinitis pigmentosa have been investigated regarding their copper metabolic state. It is observed that these patients show a normal or near normal serum copper concentration, very low plasma caeruloplasmin concentration, and a very high copper urinary excretion. A similarity between this condition and hepatolenticular degeneratio...

Journal: :Orphanet Journal of Rare Diseases 2006
Christian Hamel

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 ...

Journal: :Australian and New Zealand Journal of Ophthalmology 1982

2016

blood and urine analyses made by Dr. John M. Swan which are of interest, but which throw no fresh light on the cause or diagnosis of the disease. Retinitis Pigmentosa sine pigmento of which one frequently hears, the author regards as merely an early stage of the disease, and states that in such cases the pigments will appear sooner or later. The disease is so constantly bilateral that limitatio...

2015
RUI HUA KANG CHEN YUEDONG HU XINLING WANG LEI CHEN

Choroidal neovascularization secondary to retinitis pigmentosa is rarely observed in clinical practice. The present study describes a case of atypical retinitis pigmentosa, crystalline retinal pigmentary degeneration, complicated by choroidal neovascularization (CNV) in a 26-year-old man presenting with blurred vision in the right eye. Heidelberg multimodality imaging was performed to achieve a...

Journal: :Proceedings of the Royal Society of Medicine 1937

Journal: :Progress in Retinal and Eye Research 2018

2017
Mioara-Laura Macovei Maria-Alexandra Nica

The authors presented a clinical case of retinitis punctate albescens in a 26-year-old female patient, with a family history of typical retinitis pigmentosa (father) and bilateral cystoid macular edema treated with anti-VEGF (bevacizumab).

Journal: :American journal of ophthalmology 1975
K Fujimura Y Tsuchida Y Morita J H Jacobson

The visually evoked response (VER) to dim lights with intensities within the scotopic or lower mesopic range increased in amplitude during the progressive dark adaptation. The VER amplitude vs. time curve resembled the psychophysical dark adaptation curve. The spectral sensitivity curve of the dark-adapted VER matched the C.I.E. scotopic sensitivity curve. The dark-adapted VER was abnormal in p...

2015
Guohong Gao Chaohu Ouyang Jinhui Dai Feng Xue Xiaoying Wang Leilei Zou Minjie Chen Fei Ma Manrong Yu

BACKGROUND Low vision, along with cataract, trachoma, onchocerciasis, childhood blindness and refractive error, is one of the priorities in the global initiative, VISION 2020-The Right to Sight. The purpose of this study was to characterize the traits of patients presenting at a low vision clinic in China. METHODS A retrospective study was conducted of the records of 299 patients who visited ...

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