North Carolina macular dystrophy: clinicopathologic correlation.
نویسندگان
چکیده
PURPOSE To describe the clinical and histopathologic findings in a 72-year-old woman with North Carolina macular dystrophy. METHODS Clinical examination was performed by slit-lamp biomicroscopy, indirect ophthalmoscopy, color fundus photography, and focal electroretinography. Histopathologic examination of the enucleated left eye consisted of light microscopy. RESULTS Light microscopy demonstrated a discrete macular lesion characterized by focal absence of photoreceptor cells and retinal pigment epithelium. Bruch's membrane was attenuated in the center of the lesion and associated with marked atrophy of the choriocapillaris. Adjacent to the central lesion, some lipofuscin was identified in the retinal pigment epithelium. CONCLUSIONS North Carolina macular dystrophy has both clinical and microscopic appearances of a well-demarcated retinal and pigment epithelial lesion confined to the macula. This is consistent with the clinical impression that it is a focal macular dystrophy.
منابع مشابه
North Carolina macular dystrophy phenotype in France maps to the MCDR1 locus.
PURPOSE To determine if a family in France, which manifests an autosomal dominant macular dystrophy, has North Carolina macular dystrophy (MCDR1) and to determine its possible molecular genetic relationship with the original North Carolina family. METHODS A family from Northern France with a macular dystrophy underwent comprehensive ophthalmic examinations and were ascertained for genetic stu...
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ورودعنوان ژورنال:
- American journal of ophthalmology
دوره 132 6 شماره
صفحات -
تاریخ انتشار 2001