Case report reveals subtle OCT changes in an 8-year-old girl with stargardt disease, suggesting the importance of early detection in inherited macular dystrophies.
Stargardt disease (STGD1) is among the most prevalent inherited macular dystrophies, characterized by typical flavimaculatus flecks and varying degrees of macular atrophy. This case report highlights the importance of optical coherence tomography (OCT) to detect subtle OCT changes in an 8-year-old girl without any detectable fundus abnormalities.
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Kartı et al. (2025) studied this question.
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