Handbook of Pediatric Retinal OCT and the Eye-Brain Connection

Description:

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.

Table Of Contents:

1 Introduction to OCT Imaging in Infants and Children

2 Basic Principles of OCT and OCTA Imaging of Infants and Children

3 Optimizing Systems and Setup for OCT and OCTA Imaging of Children and Infants in the Nursery, Clinic, and Operating Room

4 OCT and OCTA Image Capture in the Nursery, Clinic, and Operating Room

5 Analyzing Structural Optical Coherence Tomography Images

6 Identifying Artifacts and Outliers in Structural Optical Coherence

7 Analyzing Optical Coherence Tomography Angiography

8 Identifying Artifacts in OCT Angiography

9 Introduction to Age-Dependent Features in Pediatric OCT Imaging

10 Foveal Development

11 Development of Retinal and Choroidal Vasculature and Peripheral

12 Vitreoretinal Abnormalities

13 Normal Optic Nerve Head: Anatomy and Development

14 Optic Nerve Head Abnormalities

15 Introduction to Research in Pediatric OCT Imaging

16 Considerations for Neonates and Children as a Vulnerable Research Population

17 Benefit of Nondilated Imaging

18 Quality Assessment

19 Reproducibility of Imaging and Interpretation

20 Secure OCT Data Storage and Networking

21 Best Disease

22 Stargardt Disease (and Fundus Flavimaculatus)

23 Retinitis Pigmentosa

24 Other Forms of Retinitis Pigmentosa-Usher Syndrome, Leber Congenital Amaurosis, and Bardet-Biedl Syndrome

25 Albinism

26 X-Linked Juvenile Retinoschisis

27 Other Inherited Retinal Diseases

28 Retinopathy of Prematurity

29 Familial Exudative Vitreoretinopathy and Norrie Disease

30 Incontinentia Pigmenti

31 Coats Disease and Coats Plus Syndrome

32 Sickle Cell Retinopathy

33 Epiretinal Membrane

34 Infectious Retinitis: TORCH Syndrome

35 White Dot Syndromes

36 Choroidal Granulomas: Tuberculosis and Sarcoidosis

37 Pediatric Intermediate Uveitis

38 Vogt-Koyanagi Harada Syndrome

39 Inflammatory and Idiopathic Choroidal Neovascularization

40 Nonaccidental Trauma

41 Ocular Injury

42 Traumatic Macular Hole

43 Commotio Retinae, Choroidal Rupture, and Sclopetaria

44 Retinal Laser Injury

45 Retinal Detachment and Proliferative Vitreoretinopathy

46 Retinoblastoma

47 Diffuse Choroidal Hemangioma

48 Circumscribed Choroidal Hemangioma

49 Choroidal Osteoma

50 Combined Hamartoma of the Retina and Retinal Pigment Epithelium

51 Retinal Astrocytic Hamartoma

52 Retinal Capillary Hemangioblastoma

53 Choroidal Nevus and Congenital Hypertrophy of the Retinal Pigment Epithelium

54 Persistent Fetal Vasculature

55 Chorioretinal Coloboma

56 Myelinated Nerve Fiber Layer

57 Torpedo Maculopathy

58 Pathologic Myopia

59 Optic Nerve Pit

60 Optic Nerve Coloboma

61 Morning Glory

62 Optic Nerve Hypoplasia

63 Tilting of the Disc and Megalopapilla

64 Optic Atrophy

65 Optic Nerve Glioma

66 Papilledema and Disc Swelling Versus Traction Elevation

67 Optic Neuritis and Multiple Sclerosis

68 Neuroretinitis

69 Optic Nerve Head Drusen

70 Childhood Glaucoma