Fundus Flavimaculatus is a genetic eye disorder that affects the retina, specifically the macula (the area responsible for sharp, central vision).
It is characterized by the appearance of scattered, yellow-white, “fish-tail” shaped flecks across the back of the eye. These flecks are actually toxic deposits of a fatty byproduct called lipofuscin. As these deposits build up, they slowly destroy the light-sensitive photoreceptor cells, leading to a progressive loss of central vision.
Fundus Flavimaculatus is considered a variant of Stargardt Disease. Both are typically caused by a mutation in the ABCA4 gene.
Vision loss is painless but progressive. Peripheral (side) vision usually remains completely normal.
A blurry, gray, or dark blind spot develops in the center of your vision. It becomes increasingly difficult to recognize faces, read small print, or watch television.
A hallmark symptom. When moving from a bright environment into a dark room (like walking into a movie theater), it takes an abnormally long time for the eyes to adjust and see clearly.
As the cone cells in the macula deteriorate, colors may begin to look washed out, faded, or difficult to distinguish from one another.
For patients with Age-Related Macular Degeneration (AMD), eye doctors often prescribe high-dose eye vitamins (AREDS2). If you have Fundus Flavimaculatus or Stargardt Disease, you MUST avoid these supplements.
Why? The genetic mutation in this disease prevents the eye from properly processing Vitamin A. If you take Vitamin A supplements, it accelerates the buildup of toxic lipofuscin in the retina, causing you to lose your vision much faster.
While there is currently no cure, proactive management is essential to maximize your remaining vision.
This specialized imaging technique acts like a blacklight for the retina. It causes the toxic lipofuscin flecks to glow brightly, allowing Dr. Fouladian to accurately map the extent of the disease and track its progression.
Confirming the exact gene mutation (usually ABCA4) is crucial. We work with specialists to facilitate genetic testing, which confirms the diagnosis and qualifies you for future clinical trials and gene therapies.
A diagnosis of an inherited retinal disease can be overwhelming. Schedule a comprehensive evaluation with Dr. Fouladian to discuss your imaging, management plan, and future options.