Results 181 to 190 of about 29,682 (236)

Genetics of the Retinal Dystrophies

open access: yes, 2018
Merepa, S   +3 more
openaire   +1 more source

Retinal capillaritis in a CRB1-associated retinal dystrophy

open access: yesOphthalmic Genetics, 2017
Purpose: To report a case of CRB1-associated retinal dystrophy characterized by vitritis, retinal capillaritis, and cystoid macular edema (CME). Methods: A case report.
Vittoria Murro   +2 more
exaly   +5 more sources

Prevalence of Generalized Retinal Dystrophy in Denmark

open access: yesOphthalmic Epidemiology, 2014
PURPOSE: Generalized retinal dystrophy is a frequent cause of visual impairment and blindness in younger individuals and a subject of new clinical intervention trials.
Hanne Jensen, Thomas Rosenberg
exaly   +2 more sources

OUTER RETINAL TUBULATION IN RETINAL DYSTROPHIES

Retina, 2017
To evaluate the occurrence and characteristics of outer retinal tubulation (ORT) in an Indian population with retinal dystrophies.In this retrospective study, 309 eyes of 157 patients with retinal dystrophies including retinitis pigmentosa (RP, 183 eyes), Stargardt disease (STGD, 93 eyes) and Best disease (33 eyes) were reviewed.
Imoro Z, Braimah   +2 more
openaire   +2 more sources

Retinitis Pigmentosa and Other Dystrophies

2010
Retinitis pigmentosa (RP) is a heterogeneous group of inherited retinal degenerations characterized by progressive degeneration of rod and cone cells that affects predominantly peripheral visual fields. Macular edema may cause additional central visual acuity decrease. Cystoid macular edema (CME) is one of the few treatable causes of visual loss in RP.
José, Sahel   +3 more
openaire   +3 more sources

Pericentral Retinal Dystrophy

Acta Ophthalmologica, 1987
Abstract. A diagnosis of pericentral retinal dystrophy was made in 28 patients from four families, all living in North Norway. Patients from two and three generations were examined, establishing the relatively benign but progressive course of the disease. The advanced stage of pericentral retinal dystrophy could not be differentiated from the advanced
openaire   +2 more sources

Retinal Dystrophy in Jeune's Syndrome

Archives of Ophthalmology, 1987
Jeune's syndrome is an autosomal-recessive condition characterized by multiple organ abnormalities, the most severe of which affect the skeleton, kidneys, and eyes. Severe respiratory insufficiency frequently results in death in infancy, but several patients have been reported to survive to adulthood.
D J, Wilson, R G, Weleber, R K, Beals
openaire   +2 more sources

Inner Retinal Function in Hereditary Retinal Dystrophies

Cells Tissues Organs, 1998
Hereditary retinal dystrophies are most often disorders of photoreceptors and/or the retinal pigment epithelium. Structures secondary to the photoreceptor layer such as bipolar, horizontal, amacrine and ganglion cells are secondarily involved. In later stages of the disease a mild to moderate loss of inner retina occurs, but the second and third ...
K, Ruether, U, Kellner
openaire   +2 more sources

Retinal Dystrophy in the Cardiofaciocutaneous Syndrome

Journal of Pediatric Ophthalmology & Strabismus, 1993
The cardiofaciocutaneous syndrome was first described by Reynolds and co-workers in 1986. x Patients have a characteristic facial appearance, mental retardation, abnormal skin and hair, and congenital heart disease. Typical facial characteristics consist of a high forehead with bitemporal narrowing, downslanting of the palpebral fissures, a depressed ...
Dunya, Ibrahim   +2 more
openaire   +3 more sources

Anti-VEGF and Retinal Dystrophies

Current Drug Targets, 2020
The therapeutic approach based on anti-vascular endothelial growth factor (anti-VEGF) molecules can be used to treat two important complications of retinal dystrophies: choroidal neovascularization and macular edema. The macular involvement in retinal dystrophies can lead to further visual deterioration in patients at a young age and already affected
Battaglia Parodi Maurizio   +2 more
openaire   +3 more sources

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