Corneal dystrophy: Difference between revisions

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Revision as of 16:20, 19 January 2010

Corneal dystrophy
MeSH D003317

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Please Take Over This Page and Apply to be Editor-In-Chief for this topic: There can be one or more than one Editor-In-Chief. You may also apply to be an Associate Editor-In-Chief of one of the subtopics below. Please mail us [2] to indicate your interest in serving either as an Editor-In-Chief of the entire topic or as an Associate Editor-In-Chief for a subtopic. Please be sure to attach your CV and or biographical sketch.


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

Other conditions affecting cornea

References

  1. 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.
  2. 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

Template:Human corneal dystrophy

Template:Congenital malformations and deformations of eye

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