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Today : Wed, 27 Aug 2008
View other Common Causes of Vision Impairment
Stargardt’s disease is a condition that affects the macula, the central region of the retina. It causes blurred sight, sensitivity to glare, and blind spots in the central visual field. The symptoms generally develop between the ages of eight to twenty years of age and it can be difficult to diagnose this condition in the early stages of the disease. Specialized electrodiagnostic tests may be required to make the diagnosis. The symptoms of Stargardt’s disease are progressive until the visual acuity reaches 20/200 to 20/400. It is an inherited condition that affects males and females equally and there is no predilection for any ethnicity. Patients with Stargardt’s do not completely lose their vision and they respond extremely well to low vision aids.
The retina is the light sensing tissue of the eye that is responsible for vision. It consists of millions of cells that absorb light and send information to the visual centers of the brain. The centermost region of the retina is called the macula and consists of light receptor cells called cone cells. The cone cells provide detailed sight, color vision, contrast vision, and daylight vision. The macula compromises less than 10 percent of the entire retina and is analogous to a “bull’s eye” in a dartboard. Surrounding the macula are rod cells, which extend to the outer peripheral edges of the retina. The rod cells are responsible for night vision, peripheral vision, and provide the brain with information that helps with orientation and mobility.
Stargardt’s disease primarily affects the cone cells of the macula, causing blurred sight, sensitivity to bright light and reduced contrast vision. In the early stages of the disease, children may have difficulty reading the chalkboard and their grades may suddenly suffer. Squinting the eyes, sitting closer to the television, or holding their reading material close to their eyes are also common symptoms. Their visual acuity may measure 20/40 (able to read a 1 inch letter from 20 feet). As the disease progresses, the visual acuity may rapidly deteriorate to 20/200 (able to read a 4 inch letter from 20 feet). Fortunately, the sight does not change much after this point. Adults with Stargardt’s disease may have blind spots in their central vision and they may also have difficulty discriminating colors. Fortunately, Stargardt’s only affects the central region of the retina and patients have excellent peripheral vision and do not become totally blind.
Stargardt’s has been linked to a defect on a gene called ABC-R, which is responsible for providing the cone cells with energy. The reduced function of the gene affects metabolic processes, which eventually lead to the death of the cone cells. The defective gene is inherited in an autosomal recessive manner, which suggests that both parents must be carriers of the defective gene and their children have a 25 percent probability of inheriting the condition. There is no medical treatment to reverse the damage caused by this gene at the present time.
Patients with Stargardt’s respond extremely well to low vision aids. Because this disease only affects the central region of the retina, optical aids can displace the image on the healthy regions of the retina. Specialized glasses, bioptic telescopes, filters, and computer technology are extremely helpful in improving the sight of those with Stargardt’s disease. Most students with Stargardt’s are able to access print visually and adults frequently are able to meet the visual criteria for driving when they wear specialized low vision spectacles.
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The Dr. Bill Takeshita Fundation
c/o The Center for the Partially Sighted
12301 Wilshire Boulevard, Suite 600
Los Angeles, CA 90025
Phone: (310) 458-3501 · Fax: (310) 458-8179
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