FECD1 (medical condition): A rare inherited eye disorder involving degeneration of the inner (epithelial) layer of the cornea. In type 1, onset occurs early in life (from early childhood) and usually takes about 20 years to affect vision.
See also:
Corneal dystrophy, Fuchs' endothelial, 1:
»Introduction: Corneal dystrophy, Fuchs' endothelial, 1
»Symptoms of Corneal dystrophy, Fuchs' endothelial, 1
FECD1: Another name for Corneal dystrophy, Fuchs' endothelial, 1 (or close medical condition association).
»Introduction: Corneal dystrophy, Fuchs' endothelial, 1
»Symptoms of Corneal dystrophy, Fuchs' endothelial, 1
Some of the symptoms of FECD1 incude:
See full list of 9 symptoms of FECD1 (Corneal dystrophy, Fuchs' endothelial, 1)
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