Copyright 2015 American Medical Association. All rights reserved. Cone and Rod Loss in Stargardt Disease Revealed by Adaptive Optics Scanning Light Ophthalmoscopy Hongxin

Cone Photoreceptor Abnormalities Correlate with Vision Loss in Patients with Stargardt Disease Yingming Chen,1 Kavitha Ratnam,2 Sanna M. Sundquist,2 Brandon Lujan,3 Radha

stargardtsconnected.org.uk [email protected] Whilst this information has kindly been provided by researchers and medical experts; overall, the evidence to support a

untitledPedro Cuevas,1 Luis A Outeiriño,2 Javier Angulo,1 Guillermo Giménez-Gallego3 1Departamento de Investigación, IRYCIS, Hospital Universitario Ramón

160 2 Hereditary Retinal and Allied Diseases Although it had been strongly stated that Star- gardt’s disease [1] and fundus flavimaculatus [2] are the same entity based

MEDICAL POLICY - GENETIC TESTING FOR RETINAL DYSTROPHIESMedical Policy Joint Medical Policies are a source for BCBSM and BCN medical policy information only. These documents

untitledCOVER STORY leading cause of central visual loss among the elderly population in the developed world. The non-neovascular form is characterized by mac- ular drusen

Prospective Cohort Study of Childhood-Onset Stargardt Disease: Fundus Autofluorescence Imaging, Progression, Comparison with Adult-Onset Disease, and Disease SymmetryS Accepted

Heritable Disorders of RPE, Bruch’s Membrane, and the Choriocapillaris Arlene V. Drack This chapter covers disorders characterized by ophthalmo- scopically visible