Superior limbic keratoconjunctivitis
Other Names for this Disease
- Theodores superior limbic keratoconjunctivitis
- Theodores syndrome
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eye disease which affects the superior bulbar conjunctiva (the clear layer that covers the eyeball, over the sclera) and tarsal conjunctiva (the clear layer that lines the eyelids), as well as the superior limbic aspect of the cornea (the area above the cornea). It is commonly found in women 20-70 years of age. The signs and symptoms include burning, redness and irritation and tend to develop slowly over a period of 1 to 10 years. Vision usually remains intact. While the underlying cause of SLK remains unknown, there appears to be an association between the condition and thyroid abnormalities (usually hyperthyroidism), contact lens wear, graft versus host disease, and preservatives from ophthalmologic medications.Superior limbic keratoconjunctivitis (SLK) is a chronic and recurrent
Last updated: 7/24/2012
- Kabat AG. Lacrimal occlusion therapy for the treatment of superior limbic keratoconjunctivitis. Optom Vis Sci. 1998; http://www.ncbi.nlm.nih.gov/pubmed/9798210. Accessed 7/23/2012.
- Oakman JH. Superior Limbic Keratoconjunctivitis. Medscape Reference. August 26, 2011; http://emedicine.medscape.com/article/1194578-overview. Accessed 7/23/2012.
- Papaliodis GN. Superior Limbic Keratoconjunctivitis. The Ocular Immunology and Uveitis Foundation. http://www.uveitis.org/docs/dm/superior_limbal_keratoconjunctivitis.pdf. Accessed 7/23/2012.
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