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From Wikipedia, the free encyclopedia. American adventure military science fiction franchise. For the film, see Stargate film.
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Main article: Stargate film. Main article: Stargate SG Main article: Stargate Atlantis. Main article: Stargate Universe.
Main article: Stargate Origins. Main article: Stargate Infinity. Main articles: Stargate fandom , List of awards and nominations received by Stargate SG-1 , List of awards and nominations received by Stargate Atlantis , and List of awards and nominations received by Stargate Universe.
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On this page:. At a glance: Stargardt Disease Symptoms:. Vision loss in childhood or adolescence, light sensitivity, color blindness.
Low vision aids, wearing dark glasses outdoors, avoiding tobacco, occupational therapy. What is Stargardt disease? What are the symptoms of Stargardt disease?
What causes Stargardt disease? Fundus autofluorescence image of a patient with Stargardt disease. How is Stargardt disease inherited?
How will my eye doctor check for Stargardt disease? Visual fields testing attempts to measure distribution and sensitivity of field of vision.
These photos may reveal the presence of lipofuscin deposits. In fundus autofluorescence FAF , a special filter is used to detect lipofuscin.
Lipofuscin is naturally fluorescent it glows in the dark when a specific wavelength of light is shined into the eye.
During the test, an electrode is placed on the cornea and light is flashed into the eye. Do you like the elegance of Baccarat, Roulette, Black Jack and more?
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Stargardt's is an inherited disease passed along to children when both parents carry mutations of a gene associated with vitamin A processing in the eye.
Parents can carry recessive genetic traits responsible for Stargardt's, even though they themselves may not have the disease. Researchers have found that about 5 percent of people carry gene mutations that cause inherited retinal diseases such as Stargardt's disease and retinitis pigmentosa.
However, the inheritance pattern of Stargardt's is variable, and it's possible for up to half of the children of a single affected parent to develop the condition.
Also, you can't predict how much vision a child may lose to Stargardt's disease based on the affected parent's vision loss.
Vision loss from Stargardt's generally begins to show up within the first 20 years of a young person's life, particularly in early childhood.
But it's difficult to pinpoint exactly when retinal damage will occur or how fast it will progress, because variations can occur even among family members with similar inherited tendencies.
In some cases, signs of Stargardt's disease appear in early childhood; but a person with Stargardt's particularly the fundus flavimaculatus version of the disease may reach middle age before vision problems are noticed.
Those who have the fundus flavimaculatus form of the disease, however, are likely to experience even more severe vision loss.
Symptoms of Stargardt's disease can include blurry or distorted vision, inability to see in low lighting and difficulty recognizing familiar faces.
In late stages of Stargardt's, color vision also may be lost. Some research indicates that exposure to bright light may play a role in triggering the retinal damage that occurs with Stargardt's.