Journal of Clinical and Experimental Ophthalmology
Open Access

Jorge Ribeiro Breda

Publications

• Case Report
  Fundus Autofluorescence and Enhanced Depth Imaging Spectral-Domain Optical Coherence Tomography in Hunter Syndrome-New Insights
  Author(s): Susana Costa Penas, António Augusto Magalhães, Jorge Ribeiro Breda, Francisco Miguel Cruz, Elisete Maria Brandão and Fernando Falcão Reis Susana Costa Penas, António Augusto Magalhães, Jorge Ribeiro Breda, Francisco Miguel Cruz, Elisete Maria Brandão and Fernando Falcão Reis
  
  Introduction: Hunter syndrome or mucopolysaccharidosis type II is a rare progressive multi-systemic disorder, caused by an abnormal storage of glycosaminoglycans (GAGs) in almost every cell type, including most ocular tissues [1,2]. Patients have a short life expectancy and ocular manifestations can be present early in the course of disease [1,2]. Purpose: To report the fundus autofluorescence and tomographic ocular findings in Hunter syndrome. Methods: A 18-year-old male patient with Hunter syndrome with progressive nyctalopia was submitted to color fundus photography, blue fundus autofluorescence (FAF), fluorescein angiography (FA) and spectral domain optical coherence tomography with enhanced-depth imaging (EDI-SD OCT). Results and discussion: Fundus examination and wide-field fluorescein angiogram revealed normal optic discs and b.. View More»
  DOI: 10.4172/2155-9570.1000577

  Abstract PDF

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