Corneal dystrophy: Difference between revisions
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==Overview== | |||
'''Human corneal dystrophies''' is a group of disorders, characterised by a noninflammatory, inherited, bilateral opacity of the transparent front part of the human [[eye]] called the ''[[cornea]]''. There is a number of rare forms varying in expression and degree of vision loss.<!-- | '''Human corneal dystrophies''' is a group of disorders, characterised by a noninflammatory, inherited, bilateral opacity of the transparent front part of the human [[eye]] called the ''[[cornea]]''. There is a number of rare forms varying in expression and degree of vision loss.<!-- | ||
Latest revision as of 19:20, 4 November 2015
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Human corneal dystrophies is a group of disorders, characterised by a noninflammatory, inherited, bilateral opacity of the transparent front part of the human eye called the cornea. There is a number of rare forms varying in expression and degree of vision loss.[1]
The International Committee for Classification of Corneal Dystrophies (IC3D) was established in 2005 and created a new classification system employing the latest data of molecular biology an genetics.[2]
List
- Fuchs' dystrophy
- Macular corneal dystrophy
- Reis-Bucklers corneal dystrophy (CDB1)
- Thiel-Behnke dystrophy (CDB2)
- Meesmann juvenile epithelial corneal dystrophy (MECD, Stocker-Holt dystrophy, OMIM 122100)
- Gelatinous drop-like corneal dystrophy
- Subepithelial mucinous corneal dystrophy
- Lisch epithelial dystrophy
- Granular corneal dystrophy type I
- Granular corneal dystrophy type II (also Avellino corneal dystrophy)
- Lattice corneal dystrophy type I
- Lattice corneal dystrophy type II
- Fleck dystrophy
- Schnyder corneal dystrophy
- Posterior amorphous corneal dystrophy
- Congenital stromal dystrophy (CSCD)
- Posterior polymorphous dystrophy type 1
- Posterior polymorphous dystrophy type 2
- Posterior polymorphous dystrophy type 3
- Congenital endothelial dystrophy type 1 (CHED1)
- Congenital endothelial dystrophy type 2 (CHED2)
- X-linked endothelial corneal dystrophy
- Epithelial basement membrane dystrophy (OMIM 121820), called a corneal dystrophy but in reality this condition is not inherited in the majority of cases, representing a non-specific reaction to a variety of corneal insults.[1]
Other conditions affecting cornea
References
- ↑ 1.0 1.1 Klintworth GK (2009). "Corneal dystrophies". Orphanet J Rare Dis. 4: 7. doi:10.1186/1750-1172-4-7. PMC 2695576. PMID 19236704.
- ↑ Weiss JS, Møller HU, Lisch W, Kinoshita S, Aldave AJ, Belin MW, Kivelä T, Busin M, Munier FL, Seitz B, Sutphin J, Bredrup C, Mannis MJ, Rapuano CJ, Van Rij G, Kim EK, Klintworth GK (2008). "The IC3D classification of the corneal dystrophies". Cornea. 27 Suppl 2: S1–83. doi:10.1097/ICO.0b013e31817780fb. PMID 19337156. Unknown parameter
|month=ignored (help)
External links
- The IC3D Classification of the Corneal Dystrophies (PDF) - The Cornea Society website.
Template:Human corneal dystrophy