Fenótipo clínico incomum da doença de Stargardt
Abstract
Mutations in the ABCA4 gene are a common cause of Stargardt disease; however, other retinal phenotypes have also been associated with mutations in this gene. We describe an observational case report of an unusual clinical phenotype of Stargardt disease. The ophthalmological examination included best corrected visual acuity, color and autofluorescence photography, fluorescein angiography, optical coherence tomography, and electrophysiology tests....
Paper Details
Title
Fenótipo clínico incomum da doença de Stargardt
Published Date
Jan 1, 2021
Volume
84
Issue
4
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History