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Chapter 7 - Diseases of the eye and adnexa (H00-H59)»Disorders of sclera, cornea, iris and ciliary body (H15-H22)»Endothelial corneal dystrophy (H18.51)

H18.51

Endothelial corneal dystrophy

Related indications (MeSH) (2)

Fuchs' Endothelial Dystrophy19 drugs (9 approved, 10 experimental)

Disorder caused by loss of endothelium of the central cornea. It is characterized by hyaline endothelial outgrowths on Descemet's membrane, epithelial blisters, reduced vision, and pain.

A grouping of three closely linked conditions: iris nevus (or Cogan-Reese) syndrome, Chandler Syndrome, and essential (progressive) iris atrophy. The most common features of this syndrome are the movement of endothelial cells off the cornea onto the iris leading to corneal swelling, distortion of the iris, and variable degrees of distortion of the pupil. The abnormal cell movement plugs fluid outflow channels of the eye causing GLAUCOMA.