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KMID : 0378019870300020107
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New Medical Journal
1987 Volume.30 No. 2 p.107 ~ p.109
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A Case of Lattice Corneal Dystrophy
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Abstract
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Lattice corneal dystrophy, a rare genetically determined human disease, is inherited as ari auto:omal dominant trait and is manifest clinically by progressive corneal opacities.
The characteristic corneal findings are the translucent, refractile lines (lattice lines) and the discrete which dots between the lattice lines in the anterior stroma of central cornea.
We experienced a case of lattice corneal dystrophy in a 63 year-old female and presented a brief review of the literatures.
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FullTexts / Linksout information
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Listed journal information
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