Lattice corneal dystrophy type 3A
Other Names for this Disease
- Lattice corneal dystrophy type III A
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cornea. It is characterized primarily by protein clumps in the clear, outer covering of the eye which cloud the cornea and impair vision. Affected people also experience recurrent corneal erosion (separation of certain layers of the cornea), which is associated with severe pain and sensitivity to bright light. Lattice corneal dystrophy type 3A is caused by changes (mutations) in the TGFBI gene and is inherited in an autosomal dominant manner. The condition is usually treated surgically.Lattice corneal dystrophy type 3A is rare condition that affects the
Last updated: 3/24/2016
- CORNEAL DYSTROPHY, LATTICE TYPE IIIA. OMIM. July 2015; http://www.omim.org/entry/608471.
- Jung JW, Kim SA, Kang EM, Kim TI, Cho HS, Kim EK. Lattice corneal dystrophy type IIIA with hyaline component from a novel A620P mutation and distinct surgical treatments. Cornea. December 2014; 33(12):1324-1331.
- Natalie A Afshari, MD, MA, FACS. Lattice Corneal Dystrophy. Medscape Reference. September 2014; http://emedicine.medscape.com/article/1193793-overview.
- The National Eye Institute (NEI) was established by Congress in 1968 to protect and prolong the vision of the American people. Click on the link to view information on this topic.
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- Online Mendelian Inheritance in Man (OMIM) is a catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine.
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