Abstract
A 43-year-old woman diagnosed with granular corneal dystrophy (GCD) type 2 on the basis of bilateral granular deposition in the corneal stroma (Fig. 1A) and the detection of a heterozygous R124H mutation of the transforming growth factor–β–induced gene (TGFIB) presented with ocular pain and conjunctival hyperemia in her left eye. Slitlamp examination showed swelling and congestion of the left conjunctiva associated with yellowish-white deposits in the bulbar region (Fig. 1B). Two weeks later, similar conjunctival lesions appeared in the lower portion of her right eye.
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