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Indian J Ophthalmol ; 2010 Jul; 58(4): 328-329
Article in English | IMSEAR | ID: sea-136082

ABSTRACT

An eight-year-old girl, an offspring of a consanguineous marriage presented with multiple anterior stromal geographic corneal opacities in both eyes. She was diagnosed to have superficial variant of granular dystrophy based on the family history, clinical features and mutation of TGF B1 gene. She was treated by alcohol-assisted removal of epithelium followed by mechanical debridement of abnormal deposits. Postoperatively, the cornea in both eyes was clear with no trace of opacity and the patient had an unaided visual acuity of 20/20 partial.


Subject(s)
Amino Acid Substitution , Anti-Bacterial Agents/therapeutic use , Child , Corneal Dystrophies, Hereditary/drug therapy , Corneal Dystrophies, Hereditary/genetics , Corneal Dystrophies, Hereditary/surgery , Debridement/methods , Female , Genetic Variation , Homozygote , Humans , Male , Mutation , Ofloxacin/therapeutic use , Siblings , Transforming Growth Factor beta1/genetics , Treatment Outcome , Visual Acuity
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