Fabry Disease: A Disorder of Childhood Onset Raphael Schiffmann, MD, MHSc, Markus Ries, MD, PhD, MHSc Pediatric Neurology Volume 64, Pages 10-20 (November 2016) DOI: 10.1016/j.pediatrneurol.2016.07.001 Copyright © 2016 Elsevier Inc. Terms and Conditions
Figure 1 Angiokeratoma on the back of a male patient. (The color version of this figure is available in the online edition.) Pediatric Neurology 2016 64, 10-20DOI: (10.1016/j.pediatrneurol.2016.07.001) Copyright © 2016 Elsevier Inc. Terms and Conditions
Figure 2 Cornea verticillata in a heterozygote female with Fabry disease. Courtesy Dr. Janine Smith. (The color version of this figure is available in the online edition.) Pediatric Neurology 2016 64, 10-20DOI: (10.1016/j.pediatrneurol.2016.07.001) Copyright © 2016 Elsevier Inc. Terms and Conditions
Figure 3 T1-weighted magnetic resonance imaging of the brain of a 28-year-old man with a history of repeated strokes since age 14 years despite three years of enzyme replacement. Old lacunar infarcts are seen, including internal capsule, right thalamus, and a more recent lacunar infarct in the proximal right optic radiations. (The color version of this figure is available in the online edition.) Pediatric Neurology 2016 64, 10-20DOI: (10.1016/j.pediatrneurol.2016.07.001) Copyright © 2016 Elsevier Inc. Terms and Conditions