Optical Coherence Tomography (OCT) plays a vital role in pediatric retina diagnosis, often revealing unrecognized retinal disorders and connections to brain injury, disease, and delayed neurodevelopment. Handbook of Pediatric Retinal OCT and the Eye-Brain Connection provides authoritative, up-to-date guidance in this promising area, showing how to optimize imaging in young children and infants, how to accurately interpret these images, and how to identify links between these images and brain and developmental disorders.
1. Section 1: Introduction to Pediatric Retinal OCT Imaging - p. iii 2. List of Illustrations - p. iii 3. List of Tables - p. iii 4. Chapter 1: Introduction to OCT Imaging in Infants and Children - p. iii 5. Chapter 2: Basic Principles of OCT and OCTA Imaging of Infants and Children - p. iii 6. Chapter 3: Optimizing Systems and Setup for OCT and OCTA Imaging of Children and Infants in the Nursery, Clinic, and Operating Room - p. iii 7. Chapter 4: OCT and OCTA Image Capture in the Nursery, Clinic, and Operating Room - p. iii 8. Chapter 5: Analyzing Structural Optical Coherence Tomography Images - p. iii 9. Chapter 6: Identifying Artifacts and Outliers in Structural Optical Coherence Tomography - p. iii 10. Chapter 7: Analyzing Optical Coherence Tomography Angiography - p. iii 11. Chapter 8: Identifying Artifacts in OCT Angiography - p. iii 12. Section 2: Evaluating Pediatric OCT Images: Age-Dependent Features and Common Abnormalities - p. iii 13. Chapter 9: Introduction to Age-Dependent Features in Pediatric OCT Imaging - p. iii 14. Chapter 10: Foveal Development - p. iii 15. Chapter 11: Development of Retinal and Choroidal Vasculature and Peripheral Retina - p. iii 16. Chapter 12: Vitreoretinal Abnormalities - p. iii 17. Chapter 13: Normal Optic Nerve Head: Anatomy and Development - p. iii 18. Chapter 14: Optic Nerve Head Abnormalities - p. iii 19. Section 3: Research Considerations for OCT Studies in Children - p. iii 20. Chapter 15: Introduction to Research in Pediatric OCT Imaging - p. iii 21. Chapter 16: Considerations for Neonates and Children as a Vulnerable Research Population - p. iii 22. Chapter 17: Benefit of Nondilated Imaging - p. iii 23. Chapter 18: Quality Assessment - p. iii 24. Chapter 19: Reproducibility of Imaging and Interpretation - p. iii 25. Chapter 20: Secure OCT Data Storage and Networking - p. iii 26. Section 4: Inherited Retinal Diseases - p. iii 27. Chapter 21: Best Disease - p. iii 28. Chapter 22: Stargardt Disease (and Fundus Flavimaculatus) - p. iii 29. Chapter 23: Retinitis Pigmentosa - p. iii 30. Chapter 24: Other Forms of Retinitis Pigmentosa—Usher Syndrome, Leber Congenital Amaurosis, and Bardet-Biedl Syndrome - p. iii 31. Chapter 25: Albinism - p. iii 32. Chapter 26: X-Linked Juvenile Retinoschisis - p. iii 33. Chapter 27: Other Inherited Retinal Diseases - p. iii 34. Section 5: Vitreoretinal and Vascular Diseases - p. iii 35. Chapter 28: Retinopathy of Prematurity - p. iii 36. Chapter 29: Familial Exudative Vitreoretinopathy and Norrie Disease - p. iii 37. Chapter 30: Incontinentia Pigmenti - p. iii 38. Chapter 31: Coats Disease and Coats Plus Syndrome - p. iii 39. Chapter 32: Sickle Cell Retinopathy - p. iii 40. Chapter 33: Epiretinal Membrane - p. iii 41. Section 6: Uveitis and Infectious Diseases - p. iii 42. Chapter 34: Infectious Retinitis: TORCH Syndrome - p. iii 43. Chapter 35: White Dot Syndromes - p. iii 44. Chapter 36: Choroidal Granulomas: Tuberculosis and Sarcoidosis - p. iii 45. Chapter 37: Pediatric Intermediate Uveitis - p. iii 46. Chapter 38: Vogt-Koyanagi Harada Syndrome - p. iii 47. Chapter 39: Inflammatory and Idiopathic Choroidal Neovascularization - p. iii 48. Section 7: Trauma and Retinal Detachment - p. iii 49. Chapter 40: Nonaccidental Trauma - p. iii 50. Chapter 41: Ocular Injury - p. iii 51. Chapter 42: Traumatic Macular Hole - p. iii 52. Chapter 43: Commotio Retinae, Choroidal Rupture, and Sclopetaria - p. iii 53. Chapter 44: Retinal Laser Injury - p. iii 54. Chapter 45: Retinal Detachment and Proliferative Vitreoretinopathy - p. iii 55. Section 8: Tumors and Hamartomas - p. iii 56. Chapter 46: Retinoblastoma - p. iii 57. Chapter 47: Diffuse Choroidal Hemangioma - p. iii 58. Chapter 48: Circumscribed Choroidal Hemangioma - p. iii 59. Chapter 49: Choroidal Osteoma - p. iii 60. Chapter 50: Combined Hamartoma of the Retina and Retinal Pigment Epithelium - p. iii 61. Chapter 51: Retinal Astrocytic Hamartoma - p. iii 62. Chapter 52: Retinal Capillary Hemangioblastoma - p. iii 63. Chapter 53: Choroidal Nevus and Congenital Hypertrophy of the Retinal Pigment Epithelium - p. iii 64. Section 9: Abnormalities of Development - p. iii 65. Chapter 54: Persistent Fetal Vasculature - p. iii 66. Chapter 55: Chorioretinal Coloboma - p. iii 67. Chapter 56: Myelinated Nerve Fiber Layer - p. iii 68. Chapter 57: Torpedo Maculopathy - p. iii 69. Chapter 58: Pathologic Myopia - p. iii 70. Section 10: Optic Nerve Abnormalities and Diseases - p. iii 71. Chapter 59: Optic Nerve Pit - p. iii 72. Chapter 60: Optic Nerve Coloboma - p. iii 73. Chapter 61: Morning Glory - p. iii 74. Chapter 62: Optic Nerve Hypoplasia - p. iii 75. Chapter 63: Tilting of the Disc and Megalopapilla - p. iii 76. Chapter 64: Optic Atrophy - p. iii 77. Chapter 65: Optic Nerve Glioma - p. iii 78. Chapter 66: Papilledema and Disc Swelling Versus Traction Elevation - p. iii 79. Chapter 67: Optic Neuritis and Multiple Sclerosis - p. iii 80. Chapter 68: Neuroretinitis - p. iii 81. Chapter 69: Optic Nerve Head Drusen - p. iii 82. Chapter 70: Childhood Glaucoma - p. iii 83. Index - p. iii 84. Inside Back Cover - p. iii
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Optical Coherence Tomography (OCT) plays a vital role in pediatric retina diagnosis, often revealing unrecognized retinal disorders and connections to brain injury, disease, and delayed neurodevelopment. Handbook of Pediatric Retinal OCT and the Eye-Brain Connection provides authoritative, up-to-date guidance in this promising area, showing how to optimize imaging in young children and infants, how to accurately interpret these images, and how to identify links between these images and brain and developmental disorders.
1. Section 1: Introduction to Pediatric Retinal OCT Imaging - p. iii 2. List of Illustrations - p. iii 3. List of Tables - p. iii 4. Chapter 1: Introduction to OCT Imaging in Infants and Children - p. iii 5. Chapter 2: Basic Principles of OCT and OCTA Imaging of Infants and Children - p. iii 6. Chapter 3: Optimizing Systems and Setup for OCT and OCTA Imaging of Children and Infants in the Nursery, Clinic, and Operating Room - p. iii 7. Chapter 4: OCT and OCTA Image Capture in the Nursery, Clinic, and Operating Room - p. iii 8. Chapter 5: Analyzing Structural Optical Coherence Tomography Images - p. iii 9. Chapter 6: Identifying Artifacts and Outliers in Structural Optical Coherence Tomography - p. iii 10. Chapter 7: Analyzing Optical Coherence Tomography Angiography - p. iii 11. Chapter 8: Identifying Artifacts in OCT Angiography - p. iii 12. Section 2: Evaluating Pediatric OCT Images: Age-Dependent Features and Common Abnormalities - p. iii 13. Chapter 9: Introduction to Age-Dependent Features in Pediatric OCT Imaging - p. iii 14. Chapter 10: Foveal Development - p. iii 15. Chapter 11: Development of Retinal and Choroidal Vasculature and Peripheral Retina - p. iii 16. Chapter 12: Vitreoretinal Abnormalities - p. iii 17. Chapter 13: Normal Optic Nerve Head: Anatomy and Development - p. iii 18. Chapter 14: Optic Nerve Head Abnormalities - p. iii 19. Section 3: Research Considerations for OCT Studies in Children - p. iii 20. Chapter 15: Introduction to Research in Pediatric OCT Imaging - p. iii 21. Chapter 16: Considerations for Neonates and Children as a Vulnerable Research Population - p. iii 22. Chapter 17: Benefit of Nondilated Imaging - p. iii 23. Chapter 18: Quality Assessment - p. iii 24. Chapter 19: Reproducibility of Imaging and Interpretation - p. iii 25. Chapter 20: Secure OCT Data Storage and Networking - p. iii 26. Section 4: Inherited Retinal Diseases - p. iii 27. Chapter 21: Best Disease - p. iii 28. Chapter 22: Stargardt Disease (and Fundus Flavimaculatus) - p. iii 29. Chapter 23: Retinitis Pigmentosa - p. iii 30. Chapter 24: Other Forms of Retinitis Pigmentosa—Usher Syndrome, Leber Congenital Amaurosis, and Bardet-Biedl Syndrome - p. iii 31. Chapter 25: Albinism - p. iii 32. Chapter 26: X-Linked Juvenile Retinoschisis - p. iii 33. Chapter 27: Other Inherited Retinal Diseases - p. iii 34. Section 5: Vitreoretinal and Vascular Diseases - p. iii 35. Chapter 28: Retinopathy of Prematurity - p. iii 36. Chapter 29: Familial Exudative Vitreoretinopathy and Norrie Disease - p. iii 37. Chapter 30: Incontinentia Pigmenti - p. iii 38. Chapter 31: Coats Disease and Coats Plus Syndrome - p. iii 39. Chapter 32: Sickle Cell Retinopathy - p. iii 40. Chapter 33: Epiretinal Membrane - p. iii 41. Section 6: Uveitis and Infectious Diseases - p. iii 42. Chapter 34: Infectious Retinitis: TORCH Syndrome - p. iii 43. Chapter 35: White Dot Syndromes - p. iii 44. Chapter 36: Choroidal Granulomas: Tuberculosis and Sarcoidosis - p. iii 45. Chapter 37: Pediatric Intermediate Uveitis - p. iii 46. Chapter 38: Vogt-Koyanagi Harada Syndrome - p. iii 47. Chapter 39: Inflammatory and Idiopathic Choroidal Neovascularization - p. iii 48. Section 7: Trauma and Retinal Detachment - p. iii 49. Chapter 40: Nonaccidental Trauma - p. iii 50. Chapter 41: Ocular Injury - p. iii 51. Chapter 42: Traumatic Macular Hole - p. iii 52. Chapter 43: Commotio Retinae, Choroidal Rupture, and Sclopetaria - p. iii 53. Chapter 44: Retinal Laser Injury - p. iii 54. Chapter 45: Retinal Detachment and Proliferative Vitreoretinopathy - p. iii 55. Section 8: Tumors and Hamartomas - p. iii 56. Chapter 46: Retinoblastoma - p. iii 57. Chapter 47: Diffuse Choroidal Hemangioma - p. iii 58. Chapter 48: Circumscribed Choroidal Hemangioma - p. iii 59. Chapter 49: Choroidal Osteoma - p. iii 60. Chapter 50: Combined Hamartoma of the Retina and Retinal Pigment Epithelium - p. iii 61. Chapter 51: Retinal Astrocytic Hamartoma - p. iii 62. Chapter 52: Retinal Capillary Hemangioblastoma - p. iii 63. Chapter 53: Choroidal Nevus and Congenital Hypertrophy of the Retinal Pigment Epithelium - p. iii 64. Section 9: Abnormalities of Development - p. iii 65. Chapter 54: Persistent Fetal Vasculature - p. iii 66. Chapter 55: Chorioretinal Coloboma - p. iii 67. Chapter 56: Myelinated Nerve Fiber Layer - p. iii 68. Chapter 57: Torpedo Maculopathy - p. iii 69. Chapter 58: Pathologic Myopia - p. iii 70. Section 10: Optic Nerve Abnormalities and Diseases - p. iii 71. Chapter 59: Optic Nerve Pit - p. iii 72. Chapter 60: Optic Nerve Coloboma - p. iii 73. Chapter 61: Morning Glory - p. iii 74. Chapter 62: Optic Nerve Hypoplasia - p. iii 75. Chapter 63: Tilting of the Disc and Megalopapilla - p. iii 76. Chapter 64: Optic Atrophy - p. iii 77. Chapter 65: Optic Nerve Glioma - p. iii 78. Chapter 66: Papilledema and Disc Swelling Versus Traction Elevation - p. iii 79. Chapter 67: Optic Neuritis and Multiple Sclerosis - p. iii 80. Chapter 68: Neuroretinitis - p. iii 81. Chapter 69: Optic Nerve Head Drusen - p. iii 82. Chapter 70: Childhood Glaucoma - p. iii 83. Index - p. iii 84. Inside Back Cover - p. iii
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