Cogan's Dystrophy is a disease that affects the cornea. It is commonly called Map-Dot-Fingerprint Dystrophy because of microscopic dot and fingerprint-like patterns that form within the layers of the cornea.
The cornea is comprised of five layers. Cogan's affects the superficial corneal layer called the epithelium. The epithelium's bottom, or basement layer of cells‚ becomes thickened and uneven. This weakens the bond between the cells and sometimes causes the epithelium to become loosened and slough off in areas. This problem is called corneal erosion.
Even though this
disease is commonly known as a dystrophy (a term that describes
genetic diseases), Cogan's is not necessarily an inherited problem.
It often affects both eyes and is typically diagnosed after the age
of 30. Cogan's usually becomes progressively worse with age.
Some patients with Cogan's dystrophy have no symptoms at all. The symptoms among patients may vary widely in severity and include:
The treatment for Cogan's is dependent on the severity of the problem. The first step is to lubricate the cornea with artificial tears to keep the surface smooth and comfortable. Lubricating ointments are recommended at bedtime so the eyes are more comfortable in the morning. Salt solution drops or ointments such as sodium chloride are often prescribed to reduce swelling and improve vision. Gas permeable contact lenses are occasionally fitted for patients with irregular astigmatism to create a smooth, even corneal surface and improve vision.
For patients with recurrent corneal erosion, soft, bandage contact lenses may be used to keep the eye comfortable and allow the cornea to heal. In some cases, laser treatment may beneficial. The surgeon removes the epithelium with an Excimer laser, creating a regular, smooth surface. The epithelium quickly regenerates, usually within a matter of days, forming a better bond with the underlying cell layer.
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