Can Stargardt lead to blindness?
Stargardt disease can cause color blindness, so your eye doctor may also test your color vision.
How do children get Stargardt macular degeneration?
Causes: Researchers blame a specific gene for the disease. If both parents carry one mutated form of the gene and one normal gene, their children have a 25% chance of getting the disease. Children who inherit only one mutated gene won’t get it. But they can pass it on without knowing it.
How fast does Stargardt progress?
How Fast Does Stargardt’s Progress? 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.
How does Stargardt start?
Stargardt’s disease usually occurs from an inherited recessive gene, meaning both parents carry the gene. In most cases, it is caused by mutations in the ABCA4 gene. Since two genes are required to cause Stargardt’s disease, parents may not have it themselves.
How fast does Stargardt’s progress?
How rare is Stargardt’s disease?
Stargardt’s Disease is one, and like many others, it is incurable at present. This genetic macular degeneration affects young people of under 20 years old and is hereditary. One in every 10,000 people suffer from it although they may not be aware of this until they reach old age.
Can you drive with Stargardt Disease?
These low vision optics enable you to read signs and see traffic lights in the distance. So getting a driver’s license and driving safely with Stargardt disease – even if you are legally blind – can be an option!
Is Stargardt Disease a disability?
Stargardt’s Disease – teens & adults in college Students with stargardt’s disease can sometimes be categorize has having a vision disability. Patients and students with visual disabilities need to be well informed about their rights and responsibilities, as well as the responsibilities of the colleges and universities.
What is the enfermedad de Stargardt in medical terms?
La enfermedad de Stargardt es una enfermedad ocular que produce pérdida de la visión en niños y en adultos jóvenes. Es una enfermedad hereditaria, es decir que se transmite de padres a hijos. La enfermedad de Stargardt, a menudo se denomina, distrofia macular juvenil.
Is there a genetic test for Stargardt disease?
Genetic testing may help distinguish the type of Stargardt disease a person has, and provide information about the mode of inheritance and risks to other family members. The Genetic Testing Registry (GTR) provides information about the genetic tests available for Stargardt disease.
What are the symptoms of Stargardt Eye Disease?
What are the symptoms of Stargardt disease? The most common symptom of Stargardt disease is variable, often slow loss of central vision in both eyes. People with the disease might notice gray, black, or hazy spots in the center of their vision, or that it takes longer than usual for their eyes to adjust when moving from light to dark environments.
What does the right macula look like with Stargardt disease?
Right macula of a young patient with Stargardt disease showing beaten bronze appearance, a small area of atrophy and some perifoveal flecks. Figure 2. Bull’s eye appearance of the macula in a patient with Stargardt disease