Section I: Basic Knowledge<div><br></div><div>1. Retinal Histology and Anatomical Landmarks</div><div>2. Fluorescein Angiography</div><div>3. Optical Coherence Tomography</div><div>4. Fundus Autofluorescence </div><div>5. Electroretinography</div><div>6. Electrooculography</div><div>7. Glossary of Relevant Genetic and Molecular/Cell Biology</div><div><br></div><div>Section II: X-linked Forms</div><div><br></div><div>8. X-Linked Retinitis Pigmentosa</div><div>9. X-Linked Choroideremia</div><div>10. X-Linked Juvenile Retinoschisis</div><div>11. X-Linked Ocular Albinism</div><div>12. Progressive Cone Dystrophy and Cone-Rod Dystrophy </div><div>13. Congenital Stationary Night Blindness </div><div>14. Blue Cone Monochromatism </div><div><br></div><div>Section III: Autosomal Dominant Forms</div><div><br></div><div>15. Autosomal Dominant Retinitis Pigmentosa </div><div>16. Best Vitelliform Macular Dystrophy</div><div>17. Pattern Dystrophy</div><div>18. Doyne Honeycomb Retinal Dystrophy (Malattia Leventinese, Autosomal Dominant Drusen) </div><div>19. Occult Macular Dystrophy </div><div>20. Sorsby Pseudoinflammatory Fundus Dystrophy</div>21. North Carolina Macular Dystrophy <div>22. Pigmented Paravenous Chorioretinal Atrophy (PPCRA)</div><div>23. Late-Onset Retinal Degeneration </div><div><br></div><div>Section IV: Autosomal Recessive Form</div><div><br></div><div>24. Rod Monochromatism (Achromatopsia)</div>25. Retinitis Pigmentosa (Non-syndromic)<div>26. Leber Congenital Amaurosis </div><div>27. Stargardt Disease </div><div>28. Enhanced S-Cone Syndrome (Goldmann-Favre Syndrome)</div><div>29. Best Vitelliform Macular Dystrophy </div><div><br></div><div>Section V: Systemic Disorders</div><br><div>30. Mitochondrial Disorder: Kearns-Sayre Syndrome </div><div>31. Mitochondrial Disorder: Maternally Inherited Diabetes and Deafness </div><div>32. Ciliopathy: Usher Syndrome </div><div>33. Ciliopathy: Bardet-Biedl Syndrome </div><div>34. Ciliopathy: Senior-Løken Syndrome</div><div>35. Ciliopathy: Alström Syndrome </div><div>36. Ciliopathy: Sjögren-Larsson Syndrome </div><div>37. Inborn Errors of Metabolism: Gyrate Atrophy </div><div>38. Inborn Errors of Metabolism: Pseudoxanthoma Elasticum</div><div>39. Inborn Errors of Metabolism: Refsum Disease </div><div>40. Inborn Errors of Metabolism: Bietti Crystalline Dystrophy </div><div>41. Extracellular Matrix: Alport Syndrome </div><div><br></div><div>Section VI: Phakomatoses</div><div><br></div><div>42. Von Hippel-Lindau Disease</div><div>43. Tuberous Sclerosis</div><div>44. Neurofibromatosis </div><div><br></div><div>Section VII: Phenocopies</div><div><br></div><div>45. Rubella Retinopathy</div><div>46. Syphilis</div><div>47. Autoimmune Retinopathy</div><div>48. Drug-Induced Retinal Toxicity</div><div>49. Acute Zonal Occult Outer Retinopathy (AZOOR) and Related Diseases</div><div>50. Diffuse Unilateral Subacute Neuroretinitis (DUSN)</div><br><div>Section VIII: Managing IRDs in Clinics</div><div><br></div><div>51. A Practical Approach to Retinal Dystrophies</div><div>52. Genetic Testing for Inherited Retinal Dystrophy: Basic Understanding</div>
