1. Fabry Disease

2. Fabry Disease Pattern of Inheritance

3. Clinical Manifestations of Fabry Disease

4. Recommended Schedule of Assessments for Pediatric Patients From the Fabry Registry

5. Recommended Schedule of Assessments for Adult Patients From the Fabry Registry

6. Genetic Mutations Linked to Fabry Disease

7. Enzyme Replacement Therapy (ERT)

8. Instituting ERT in Patients With Fabry Disease

9. ERT With Agalsidase Beta Ten-Year Outcome

10. Initiating ERT in Pediatric Patients With Fabry Disease

11. ATTRACT Phase 3 Study of Migalastat vs ERT

12. Abbreviations