Hyperreflective Outer Nuclear Layer as a Biomarker of Early Stargardt Disease. A Case Report
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
Autoři: Omer Karti; Ziya Ayhan; Osman Saatci Ali Působiště autorů: Dokuz Eylul University, Department of Ophthalmology, İzmir, Türkiye Vyšlo v časopise: Čes. a slov. Oftal., 81, 2025, No. Ahead of Print, p. 1-4 Kategorie: Kazuistika doi: https://doi.org/10.31348/2025/37
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