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Qu'est-ce (qui) est X-linked endothelial corneal dystrophy - définition
X-linked endothelial corneal dystrophy
HUMAN DISEASE
X-linked endothelial corneal dystrophy (XECD) is a rare form of corneal dystrophy described first in 2006, based on a 4-generation family of 60 members with 9 affected males and 35 trait carriers, which led to mapping the XECD locus to Xq25. It manifests as severe corneal opacification or clouding, sometimes congenital, in the form of a ground glass, milky corneal tissue, and moon crater-like changes of corneal endothelium.
Granular corneal dystrophy
HUMAN DISEASE
Granular corneal dystrophy type I; Granular corneal dystrophy type II; Avellino corneal dystrophy
Granular corneal dystrophy is a slowly progressive corneal dystrophy that most often begins in early childhood.
Macular corneal dystrophy
CORNEAL DYSTROPHY THAT IS CHARACTERIZED BY CORNEAL HAZE, SEVERE PHOTOPHOBIA AT NIGHT ,GRADUAL VISION IMPAIRMENT ,BILATERAL LOSS OF VISION, EVENTUALLY NECESSITATING CORNEAL TRANSPLANTATION RESULTING FROM PROGRESSIVE PUNCTATE OPACITIES IN THE CORNEA
Groenouw Type II corneal dystrophy; Fehr corneal dystrophy; Type II Groenow's dystrophy
Macular corneal dystrophy, also known as Fehr corneal dystrophy named for German ophthalmologist Oskar Fehr (1871-1959), is a rare pathological condition affecting the stroma of cornea. The first signs are usually noticed in the first decade of life, and progress afterwards, with opacities developing in the cornea and attacks of pain.
