corneal dystrophy, Groenouw type 1
corneal dystrophy, Groenouw type 1An autosomal dominant (OMIM:121900) form of corneal dystrophy characterised by progressive corneal opacification with loss of vision.
Has been linked to defects of TGFBI, which encodes an RGD protein that binds to type-I, -II and -IV collagens and plays a role in cell–collagen interactions.
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