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. Author manuscript; available in PMC: 2015 Sep 1.
Published in final edited form as: Ophthalmic Genet. 2015 Sep;36(3):244–247. doi: 10.3109/13816810.2013.848908

Table 2.

Families with corneal and lens abnormalities and MIR184 c.57C>T mutation.

# Description Ethnicity Inheritance Corneal Defects Iris Defect Lens Defect
1 Keratoconus with cataract Northern Irish Autosomal Dominant Keratoconus None Congenital polar cataract
2 EDICT ? Autosomal Dominant Corneal endothelial dystrophy; Uniform corneal thinning with uniform steepening Hypoplasia Congenital cataract
3 Keratoconus and corneal thinning with cataract Galician Autosomal Dominant Keratoconus; Extreme corneal thinning with uniform steepening None Congenital posterior cataract