Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
4024040 | Journal Français d'Ophtalmologie | 2010 | 5 Pages |
Abstract
Schnyder's crystalline corneal dystrophy is a rare bilateral hereditary disease with various clinical features. It typically presents as a central disc-like opacification with or without crystalline deposits. We report the case of a particular crystalline-free and ring-like pattern dystrophy resembling Schnyder's corneal dystrophy in an 82-year-old woman. In addition, we describe the aspects of this dystrophy with in vivo confocal microscopy using the Heidelberg Retina Tomograph II-Rostock Cornea Module and with anterior segment optical coherence tomography (OCT-Visante®). These techniques can be useful in the diagnosis or the therapeutic process, showing crystalline structures that are not clinically distinguishable or validating the histological localization of the corneal disease.
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Authors
E. Brasnu, B. Dupas, T. Hoang-Xuan, C. Baudouin, D. Gatinel,