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Groenouw corneal dystrophy

Pronunciation: gro'no


  1. a granular type of corneal dystrophy, with autosomal dominant inheritance [MIM*121900], caused by mutation in the transforming growth factor, beta-induced, gene (TGFßI) encoding keratoepithelin on chromosome 5q;
  2. a progressive macular type of corneal dystrophy, characterized by punctate opacities and episodes of photophobia, corneal erosion, and foreign body sensation; autosomal recessive inheritance.

Further information

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© Copyright 2018 Wolters Kluwer. All Rights Reserved. Review date: Sep 19, 2016.