Butterfly-Shaped Pattern Dystrophy
نویسندگان
چکیده
منابع مشابه
Butterfly-shaped pattern dystrophy in myotonic dystrophy.
A 50-year-old woman with myotonic dystrophy (MD) presented with bilateral blurred vision. Visual acuity was 16/ 20 in both eyes. Slit lamp examination showed cortical and posterior subcapsular opacities in both lenses. Funduscopy showed depigmented changes at the macula, however, details were unclear due to the presence of cataract (Picture 1). Fundus autofluorescence (FAF) imaging clearly defi...
متن کامل[Butterfly-shaped pattern dystrophy: case report].
The authors present a case of butterfly-shaped pattern dystrophy diagnosed in a male patient, with retinal pigmented epithelium atrophy and central visual acuity decrease in one of the eyes. The evolution of this case was not benign as described in previous reports. A well-defined lesion located in the posterior pole of both eyes associated with fluorescein angiography allowed the diagnosis of ...
متن کاملbutterfly-shaped macular dystrophy
purpose: to report a case of butterfly-shaped macular dystrophy. patient and findings: a 34-year-old woman presented with metamorphopsia in both eyes from 2 years ago. visual acuity was 9/10 in right eye and 10/10 in left eye. there was no pathologic finding on slit lamp biomicroscopy and funduscopy other than mild macular retinal pigment epithelium mottling. visual fields and electroretinogram...
متن کاملVitelliform macular dystrophy and butterfly-shaped epithelial dystrophy: a continuum?
We report the case of 22-year-old white female who presented for a routine ocular examination and displayed Best's disease in her right eye and butterfly-shaped macular dystrophy in her left eye. These diagnoses were confirmed by fluorescein angiography, EOG, and ERG. The fact that these 2 disorders are present in one person suggests that they are only different manifestations of the same under...
متن کاملGenetic heterogeneity of butterfly-shaped pigment dystrophy of the fovea.
PURPOSE Butterfly-shaped macular dystrophy (BSMD) has so far only been associated with mutations in the peripherin/RDS gene. The initial aim of our study was to investigate the peripherin/RDS gene as the causative gene in a family with BSMD. Subsequently the putative involvement of the ROM-1 gene, 4 genes expressed in cone photoreceptors, all known non-syndromic macular, retinal pigment epithel...
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ژورنال
عنوان ژورنال: Archives of Ophthalmology
سال: 2002
ISSN: 0003-9950
DOI: 10.1001/archopht.120.4.485