Sumit chrono
7 months ago
Stargardt disease and other macular dystrophies usually begin in childhood or the teenage years, when reading, school work and exams matter most. Because they blur central vision while the eye looks normal from outside, they are often mistaken for ordinary short sight at first. This page explains the condition and the support available.

The macula is the small centre of the retina used for reading, writing and recognising faces. In Stargardt disease, usually linked to the ABCA4 gene, waste material builds up under the macula and the cells there gradually stop working.
Side vision is usually kept, so most people can still find their way around.
These are the signs families most often describe.
Simple habits and support make a real difference.
Quality UV-blocking sunglasses and a hat help under strong equatorial sun.
Ask your doctor before taking vitamin A supplements, since high intake may not be helpful.
Sitting near the front, large print and extra time make a big difference.
Phone zoom, screen readers and high-contrast settings help many students.
Here is what to expect when you contact our team.
Autofluorescence and OCT imaging, electrical tests, and genetic testing that also helps advise brothers and sisters.
Research has focused on supporting or replacing the RPE cells under the macula. Stem cell therapy for this condition is still experimental. It is not an approved standard treatment, and results differ from person to person. We cannot promise any particular outcome.
Parents or guardians are welcome at the assessment, and we encourage young people to ask their own questions.
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Get ConsultationStargardt typically affects central vision while side vision is usually kept. Severity varies between individuals.
Usually yes, most often in a recessive pattern, so parents are often carriers without symptoms.
No. It is experimental, and any discussion is about possible benefit, not a cure.