Case report on Best vitelliform macular dystrophy: A cause of fixation disparity
نویسندگان
چکیده
Introduction: To evaluate a case of bilateral diminution vision with metamorphopsia and hyperdeviation. This is retrospective descriptive study data was gathered from series questionnaire investigative analysis. Case Report: A 27-yea
منابع مشابه
“ A Case Report on Best ’ s Vitelliform Macular Dystrophy . ”
Best’s disease also termed as vitelliform macular dystrophy is an autosomal dominant sorder which classically presents in childhood with the striking appearance of a yellow or orange yolk like lesion in the macula. Dr Franz Best, a German ophthalmologist, described the first pedigree in 1905. A 23year old male with complain of gradual reduction of vision distortion of images and presence of bli...
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Focal choroidal excavation (FCE) was first reported as a choroidal posteriorly excavated zone without any scleral change. Choroidal excavation also divided into conforming and nonconforming type. Numerous reports demonstrated association between FCE and other disease such as choroidal neovascularization and central serous choroidoretinopathy. Here, we report a rare case of FCE in a patient with...
متن کاملfluctuation of vision in best vitelliform macular dystrophy, a case report
purpose: to introduce a patient with best disease and fluctuation in vision and oct changes. case report: a 26-year-old man presented with decreased va in his left eye due to cnv secondary to best disease. va improved after ivb injection. after 3 years he complained of metamorphopsia in his right eye with a decrease in subretinal deposits which improved spontaneously. the same sequence of event...
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Best vitelliform macular dystrophy is the second most common type of hereditary fundus dystrophies. Our case report describes twin brothers of Afghan family who developed Best vitelliform macular dystrophy. One of them developed choroidal neovascularization in one eye which was treated with single intravitreal injection of bevacizumab. The patient showed stable vision and did not have any recur...
متن کاملA model of best vitelliform macular dystrophy in rats.
PURPOSE The VMD2 gene, mutated in Best macular dystrophy (BMD) encodes bestrophin, a 68-kDa basolateral plasma membrane protein expressed in retinal pigment epithelial (RPE) cells. BMD is characterized by a depressed light peak (LP) in the electro-oculogram. Bestrophin is thought to be the Cl channel that generates the LP. The goal was to generate an animal model of BMD and to determine the eff...
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ژورنال
عنوان ژورنال: International Journal of Case Reports and Images
سال: 2021
ISSN: ['0976-3198']
DOI: https://doi.org/10.5348/101198z01pk2021cr