A 16-year-old boy presents with progressive central vision loss over the past 2 years and difficulty reading. Fundoscopy reveals bilateral macular atrophy with yellow pisciform flecks at the posterior pole, as marked **A** in the diagram. Fluorescein angiography shows a dark choroid sign. Which of the following genetic mutations is most likely responsible for this presentation?
Ready to test yourself?
Test your Ophthalmology knowledge with AI-powered MCQs and detailed explanations — no signup required to try.
Sign up free and practice all 1 Stargardt Disease MCQs with AI-powered explanations tailored to your performance.
Create Free Account