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Title: [Schnyder's crystalline-like corneal dystrophy: a case report]. Author: Brasnu E, Dupas B, Hoang-Xuan T, Baudouin C, Gatinel D. Journal: J Fr Ophtalmol; 2010 Apr; 33(4):264.e1-5. PubMed ID: 20334950. 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((R))). 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.[Abstract] [Full Text] [Related] [New Search]