Pediatric Neuro-Ophthalmology

Pediatric Neuro-Ophthalmology, 3rd edition provides the single authoritative resource on the pathophysiology, diagnostic evaluation, and treatment of neuro-ophthalmologic disorders in children. This book is encyclopedic in scope, incorporating extensive references for each condition, numerous diagra...

Πλήρης περιγραφή

Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριος συγγραφέας: Brodsky, Michael C. (Συγγραφέας)
Συγγραφή απο Οργανισμό/Αρχή: SpringerLink (Online service)
Μορφή: Ηλεκτρονική πηγή Ηλ. βιβλίο
Γλώσσα:English
Έκδοση: New York, NY : Springer New York : Imprint: Springer, 2016.
Έκδοση:3rd ed. 2016.
Θέματα:
Διαθέσιμο Online:Full Text via HEAL-Link
Πίνακας περιεχομένων:
  • 1. The Apparently Blind Infant
  • Introduction
  • Hereditary Retinal Disorders
  • Leber Congenital Amaurosis
  • Joubert Syndrome
  • Congenital Stationary Night Blindness
  • Achromatopsia
  • Congenital Optic Nerve Disorders
  • Cortical Visual Insufficiency
  • Causes of Cortical Visual Loss
  • Neurologic and Systemic Disorders
  • Characteristics of Visual Function
  • Neuro-Ophthalmologic Findings
  • Diagnostic and Prognostic Considerations
  • Role of Visual Attention
  • Subcortical Visual Loss (or Periventricular Leukomalacia)
  • Neuroimaging Abnormalities and their Implications
  • Neuro-Ophthalmologic Findings
  • Perceptual Difficulties
  • Dorsal and Ventral Stream Dysfunction
  • Pathophysiology
  • Intraventricular Hemorrhage
  • Periventricular and Intraventricular Hemorrhage
  • Hemianopic Visual Field Defects in Children
  • Delayed Visual Maturation
  • Blindsight
  • The Effect of Total Blindness on Circadian Regulation
  • Horizons
  • 2. Congenital Optic Disc Anomalies
  • Introduction
  • Optic Nerve Hypoplasia
  • Excavated Optic Disc Anomalies
  • Morning Glory Disc Anomaly
  • Optic Disc Coloboma
  • Peripapillary Staphyloma
  • Megalopapilla
  • Optic Pit
  • Papillorenal Syndrome (The Vacant Optic Disc)
  • Congenital Tilted Disc Syndrome
  • Optic Disc Dysplasia
  • Congenital Optic Disc Pigmentation
  • Aicardi Syndrome
  • Doubling of the Optic Disc
  • Optic Nerve Aplasia
  • Myelinated (Medullated) Nerve Fibers
  • The Albinotic Optic Disc
  • 3. The Swollen Optic Disc
  • Papilledema
  • Idiopathic Intracranial Hypertension (IIH) in Children
  • Optic Disc Swelling Secondary to Neurological Disease
  • Optic Disc Swelling Secondary to Systemic Disease
  • Uveitis
  • Posttraumatic Optic Disc Swelling
  • Intrinsic Optic Disc Tumors
  • Optic Disc Hemangioma
  • Tuberous Sclerosis
  • Optic Disc Glioma
  • Combined Hamartoma of the Retina and RPE
  • Retrobulbar Tumors
  • Optic Neuritis in Children
  • History and Physical Examination
  • Postinfectious Optic Neuritis
  • Disseminated Encephalomyelitis
  • MS and Pediatric Optic Neuritis
  • Devic Disease (Neuromyelitis Optica)
  • Prognosis and Treatment
  • Course of Visual Loss and Visual Recovery
  • Systemic Prognosis
  • Systemic Evaluation of Pediatric Optic Neuritis
  • Treatment
  • Leber Idiopathic Stellate Neuroretinitis
  • Ischemic Optic Neuropathy
  • Autoimmune Optic Neuropathy
  • Pseudopapilledema
  • Optic Disc Drusen
  • Ocular Disorders Associated with Pseudopapilledema
  • Systemic Disorders Associated with Pseudopapilledema
  • 4. Optic Atrophy
  • Introduction
  • Optic Atrophy Associated with Retinal Disease
  • Optic Atrophy Vs. Hypoplasia
  • Causes of Optic Atrophy in Children
  • Compressive/Infiltrative Intracranial Lesions
  • Noncompressive Causes of Optic Atrophy in Children with Brain Tumors
  • Hereditary Optic Atrophy
  • Dominant Optic Atrophy (Kjer Type)
  • Leber Hereditary Optic Neuropathy
  • Recessive Optic Atrophhy
  • Behr Syndrome
  • Wolfram Syndrome (DIDMOAD)
  • Toxic/Nutritional Optic Neuropathy
  • Neurodegenerative Disorders with Optic Atrophy
  • Organic Acidurias
  • Optic Atrophy due to Hypoxia-Ischemia
  • Traumatic Optic Atrophy
  • Miscellaneous Causes
  • Summary of the General Approach to the Child with Optic Atrophy
  • 5. Transient, Unexplained, and Psychogenic Visual Loss
  • Introduction
  • Transient Visual Loss
  • Migraine
  • Epilepsy
  • Posttraumatic Transient Cerebral Blindness
  • Cardiogenic Embolism
  • Nonmigrainous Cerebrovascular Disease
  • Miscellaneous Transient Visual Disturbances in Children
  • Toxic and Nontoxic Drug Effects
  • Summary of Clinical Approach to the Child with Transient Visual Disturbances
  • Laboratory Evaluation of Transient Visual Disturbances in Children
  • Unexplained Visual Loss in Children
  • Causes of Unexplained Visual Loss in Childhood
  • Psychogenic Visual Loss in Children
  • Clinical Profile
  • Neuro-Ophthalmologic Findings
  • Categories of Psychogenic Visual Loss in Children
  • Management of Psychogenic Visual Loss in Children
  • Horizons
  • 6. Ocular Motor Nerve Palsies
  • Introduction
  • Oculomotor Nerve Palsy
  • Clinical Anatomy
  • Clinical Features
  • Partial Forms of Oculomotor Palsy
  • Oculomotor Synkinesis
  • Etiology
  • Vascular Third Nerve Palsy in Children
  • Differential Diagnosis
  • Management
  • Trochlear Nerve Palsy
  • Clinical Anatomy
  • Clinical Features
  • Bilateral Trochlear Nerve Palsy
  • Etiology
  • Differential Diagnosis
  • Treatment
  • Abducens Nerve Palsy
  • Anatomy
  • Clinical Features
  • Causes of Sixth Nerve Palsy
  • Differential Diagnosis
  • Duane Retraction Syndrome
  • Management of Sixth Nerve Pals
  • Multiple Cranial Nerve Palsies in Children
  • Horizons
  • 7. Complex Ocular Motor Disorders
  • Introduction
  • Strabismus in Children with Neurological Dysfunction
  • Visuovestibular Disorders
  • Neurologic Esotropia
  • Neurologic Exotropia
  • Skew Deviation
  • Gaze Palsies, Gaze Deviations, and Ophthalmoplegia
  • Horizontal Gaze Palsy in Children
  • Congenital Ocular Motor Apraxia
  • Vertical Gaze Palsies in Children
  • Diffuse Ophthalmoplegia in Children
  • Chronic Progressive External Ophthalmoplegia
  • Myasthenia Gravis
  • Olivopontocerebellar Atrophy
  • Botulism
  • Fisher Syndrome: A Variant of Guillain–Barré Syndrome
  • Bickerstaff Brainstem Encephalitis
  • Tick Paralysis
  • Wernicke Encephalopathy
  • Miscellaneous Causes of Ophthalmoplegia
  • Transient Ocular Motor Disturbances of Infancy
  • Transient Neonatal Strabismus
  • Transient Idiopathic Nystagmus
  • Tonic Downgaze
  • Tonic Upgaze
  • Neonatal Opsoclonus
  • Transient Vertical Strabismus in Infancy
  • Congenital Cranial Dysinnervation Syndromes
  • Congenital Ptosis
  • Marcus Gunn Jaw Winking (Trigemino-Oculomotor Synkinesis)
  • Congenital Fibrosis Syndrome
  • Congenital Horizontal Gaze Palsy with Scoliosis
  • Möbius Sequence
  • Monocular Elevation Deficiency, or “Double Elevator Palsy”
  • Brown Syndrome
  • Other Pathologic Synkineses
  • Internuclear Ophthalmoplegia
  • Cyclic, Periodic, or Aperiodic Disorders Affecting Ocular Structures
  • Ocular Neuromyotonia
  • Ocular Motor Adaptations and Disorders in Patients with Hemispheric Abnormalities
  • Movement Tics
  • Eyelid Abnormalities in Children
  • Congenital Ptosis
  • Excessive Blinking in Children
  • Hemifacial Spasm
  • Eyelid Retraction
  • Apraxia of Eyelid Opening
  • Pupillary Abnormalities
  • Congenital Bilateral Mydriasis
  • Accommodative Paresis
  • Adie Syndrome
  • Horner Syndrome
  • 8.
  • Nystagmus
  • Introduction
  • Infantile Nystagmus
  • Clinical Features
  • Onset of Infantile Nystagmus
  • Terminology
  • History and Physical Examination
  • ERG
  • Hemispheric Visual Evoked Potentials
  • Overlap of Infantile Nystagmus and Strabismus
  • Eye Movement Recordings in Infantile Nystagmus
  • Contrast Sensitivity and Pattern Detection Thresholds in Infantile Nystagmus
  • Theories of Causation
  • Visual Disorders Precipitating Infantile Nystagmus
  • When to Obtain Neuroimaging Studies in Children with Nystagmus
  • Treatment
  • Spasmus Nutans
  • Russell Diencephalic Syndrome of Infancy
  • Monocular Nystagmus
  • Nystagmus Associated with Infantile Esotropia
  • Torsional Nystagmus
  • Horizontal Nystagmus
  • Nystagmus
  • Nystagmus Blockage Syndrome
  • Treatment of Nystagmus Blockage Syndrome
  • Vertical Nystagmus
  • Upbeating Nystagmus in Infancy
  • Congenital Downbeat Nystagmus
  • Hereditary Vertical Nystagmus
  • Periodic Alternating Nystagmus
  • Seesaw Nystagmus
  • Congenital versus Acquired Seesaw Nystagmus
  • Saccadic Oscillations that Simulate Nystagmus
  • Retraction Nystagmus
  • Opsoclonus and Ocular Flutter
  • Voluntary Nystagmus
  • Ocular Bobbing
  • Neurological Nystagmus
  • Leigh Subacute Necrotizing Encephalomyelopathy
  • Pelizaeus-Merzbacher Disease
  • Joubert Syndrome
  • Santavuori-Haltia Disease
  • Infantile Neuroaxonal Dystrophy
  • Deficient Glycoprotein Syndromes
  • Down Syndrome
  • Hypothyroidism
  • Maple Syrup Urine Disease
  • Nutritional Nystagmus
  • Epileptic Nystagmus
  • Cobalamin C Methylmalonic Aciduria and Homocystinuria
  • Familial Vestibulocerebellar Disorder
  • Summary
  • 9. Torticollis and Head Oscillations
  • Introduction
  • Torticollis
  • Ocular Torticollis
  • Head Tilts
  • Head Turns
  • Vertical Head Positions
  • Refractive Causes of Torticollis
  • Neuromuscular Causes of Torticollis
  • Systemic Causes of Torticollis
  • Head Oscillations
  • Head Nodding with Nystagmus
  • Head Nodding without Nystagmus
  • Visual Disorders
  • Otological Abnormalities
  • Systemic Disorders
  • 10. Neuro-Ophthalmologic Manifestations of Neurodegenerative Disorders
  • Introduction
  • Neuronal Disease
  • Neuronal Ceroid Lipofuscinosis
  • Lysosomal Diseases
  • Gangliosidoses
  • Mucopolysaccharidoses
  • Subacute Sclerosing Panencephalitis
  • White Matter Disorders
  • Metachromatic Leukodystrophy
  • Canavan Disease (Spongy Degeneration of Cerebral White Matter)
  • Krabbe Disease
  • Pelizaeus–Merzbacher Disease
  • Cockayne Syndrome
  • Alexander Disease
  • Sjögren–Larsson Syndrome
  • Cerebrotendinous Xanthomatosis
  • Peroxisomal Disorders
  • Zellweger Syndrome
  • Adrenoleukodystrophy
  • Basal Ganglia Disease
  • Pantothenate Kinase-Associated Neurodegeneration
  • Wilson Disease
  • Aminoacidopathies and Other Biochemical Defectsl
  • Maple Syrup Urine Disease
  • Homocystinuria
  • Abetalipoproteinemia
  • Mitochondrial Encephalomyelopathies
  • Chronic Progressive External Ophthalmoplegia (CPEO)
  • Leigh Subacute Necrotizing Encephalomyelopathy
  • Mitochondrial Encephalomyelopathy and Stroke-Like Episodes (MELAS)
  • Myoclonic Epilepsy and Ragged Red Fibers (MERRF)
  • Mitochondrial Depletion Syndrome
  • Congenital Disorders of Glycosylation
  • Horizons
  • 11. Neuro-Ophthalmologic Manifestations of Systemic and Intracranial Disease
  • Introduction
  • The Phakomatoses
  • Neurofibromatosis (NF1)
  • Neurofibromatosis 2 (NF2)
  • Tuberous Sclerosis
  • Sturge–Weber Syndrome
  • von Hippel–Lindau Disease
  • Ataxia Telangiectasia
  • Linear Nevus Sebaceous Syndrome
  • Klippel.