Authors: Omer Karti; Ziya Ayhan; Osman Saatci Ali Authors‘ workplace: Dokuz Eylul University, Department of Ophthalmology, İzmir, Türkiye Published in: Čes. a slov. Oftal., 81, 2025, No. Ahead of Print, p. 1-4 Category: Case Report doi: https://doi.org/10.31348/2025/37
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.
optical coherence tomography – ABCA4 gene – flavimaculatus flecks – Stargardt disease
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