Table of Contents
Who was Stargardt?
His name is associated with Stargardt disease, an hereditary eye disease that is one of the most common causes of childhood macular degeneration….
|Born||Karl Stargardt4 December 1875|
|Died||2 April 1927 (aged 51)|
Who discovered Stargardt disease?
Stargardt’s Disease It’s named after German eye doctor Karl Stargardt, who discovered it in 1901. It affects about one in 10,000 children in the U.S. Although the disease starts before age 20, you may not notice vision loss until age 30 to 40.
When was Stargardt disease discovered?
Of those cases, the most common cause is Stargardt disease, named for Karl Stargardt, a German ophthalmologist who first reported a case in his practice in 1901.
How rare is Stargardt?
Stargardt macular degeneration is the most common form of juvenile macular degeneration, the signs and symptoms of which begin in childhood. The estimated prevalence of Stargardt macular degeneration is 1 in 8,000 to 10,000 individuals.
Is Stargardt disease genetic?
In Stargardt disease, this gene doesn’t work — so the fatty material builds up in yellowish clumps on the macula. Over time, this fatty material kills the light-sensitive cells and destroys your central vision. Stargardt disease is an inherited genetic disease, which means it gets passed down from parents to children.
How is Stargardt disease inherited?
Stargardt disease is most commonly inherited in an autosomal recessive manner. This means that to be affected, a person must have a mutation in both copies of the responsible gene in each cell . Affected people inherit one mutated copy of the gene from each parent, who is referred to as a carrier .
How many people have Stargardt’s disease?
Is Stargardt’s hereditary?
Over time, this fatty material kills the light-sensitive cells and destroys your central vision. Stargardt disease is an inherited genetic disease, which means it gets passed down from parents to children.
Will there be a cure for Stargardt?
At this time there is no treatment available for Stargardt disease. However, researchers are studying gene and drug therapies. One promising study involves delivering a healthy version of the gene that causes Stargardt disease, ABCA4, into retinal cells to restore production of the normal protein.
How rare is Stargardt disease?
How does a person with Stargardt disease see?
The most common symptom of Stargardt disease is a slow loss of central vision in both eyes. Some people lose their central vision more quickly than others. Other symptoms may include: Gray, black, or hazy spots in the center of your vision.
Is there a cure for Stargardt’s?