Sumit chrono
7 months ago
Central vision loss in young people is hard on the whole family. This page explains how Stargardt disease and related macular dystrophies are diagnosed in Dubai, and what practical care can help you or your child keep studying, working and living independently.

Fundus autofluorescence and OCT reveal the typical macular changes, and ERG shows whether the wider retina is involved. A genetic test, usually for the ABCA4 gene, confirms Stargardt disease. Other types, such as Best disease and pattern dystrophy, are identified by their own imaging signs.
Sunglasses and a brimmed hat are strongly advised given the intense UAE sunshine.
Many specialists advise against high-dose vitamin A products in Stargardt disease, so ask first.
Magnification, high-contrast settings and screen readers keep reading and work achievable.
Gene, drug and cell trials are running worldwide. Your specialist or ours can help you judge which ones are credible.
Send autofluorescence images, OCT and genetic reports through our Upload Report page. We will give you a clear view of your options, with experimental treatments always described as such.
Eye Stem Cell Center brings together pioneers in stem cell biotechnology and highly experienced ophthalmologists to provide advanced regenerative eye care with compassion and precision.
Dr. Pallavi is renowned for her expertise in cataract and corneal surgeries. With thousands of successful procedures, she combines surgical precision with a patient‑first approach.
Get ConsultationDr. Robin specializes in advanced cataract surgery, refractive procedures, and keratoconus treatment. His clinical excellence ensures patients receive world‑class eye care.
Get ConsultationDr. Pawan is an expert in retinal disorders, diabetic retinopathy, and advanced retina procedures. His patient‑focused approach ensures precise treatment and long‑term vision care.
Get ConsultationStargardt disease mainly affects central vision, and side vision is usually kept.
Not yet. Care focuses on protection, support and access to trials.
Stargardt disease is usually recessive, so children of an affected person are typically carriers. A genetics service can explain your family’s specific risk.