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IAP Textbook of Pediatric Neurology
Anoop Verma, PAM Kunju, Sujata Kanhere, Nitin Maheshwari
1:
Neurologic Assessment
INTRODUCTION
HISTORY
THE NEUROLOGICAL EXAMINATION
GENERAL EXAMINATION
HIGHER CORTICAL FUNCTION TESTS
Steps
Cranial Nerves
EXAMINING THE MOTOR SYSTEM
Muscle Wasting and Fasciculation
Muscle Tone
Power Testing
Interpretation
Grading of Weakness
Medical Research Council Scale
REFLEXES
Superficial Reflexes
Plantar Reflexes
Alternate Methods for Extensor Plantar
Release Reflexes
Gait
COORDINATION AND ABNORMAL MOVEMENT
Sensory Examination
How to Formulate the Diagnosis
Steps in Diagnosis
2:
The Child with Developmental Delay
INTRODUCTION
GLOBAL DEVELOPMENTAL DELAY
Developmental History and Clinical Evaluation
Clues from History
Localization
Central
Peripheral
EXAMINATION
General Examination
Eye and Developmental Disorders
Hair and Developmental Disorders
Microcephaly: Since Birth
Skin and Developmental Disorders
Hypopigmentation
Ichthyosis
Neurologic Examination
Developmental Examination
I. Ameil-Tison Method
II. Infant Motor Screen
Vojta Method of Early Diagnosis
DEVELOPMENTAL ASSESSMENT IN OFFICE PRACTICE
Motor Development
Fine Motor (Adaptive) Development (Table 2)
Pitfalls in Developmental Assessment
Language
Hearing
Social Development
DEVELOPMENTAL OBSERVATION CARD
Cranial Nerve Examination
Tone
Reflex Behavior
HEMISYNDROMES
Coordination and Cerebellar Signs
(i) Abnormal Movements
(ii) Soft Signs
Sensory Examination
FORMULATING THE DIAGNOSIS
Nonprogressive Central Motor Disorder (e. g. Cerebral Palsy)
Progressive Central Disorder
Peripheral Progressive Disorder
CAUSES OF DEVELOPMENTAL DELAY
Prenatal/Perinatal
Postnatal
INVESTIGATIONS
Biochemical Tests
Neuroimaging
TREATMENT
PROGNOSIS
CERTAIN ANATOMICAL PATTERNS
SOME DEVELOPMENTAL DISORDERS
Dominant Mental Developmental Delay
Chromosomal Disturbances
Autism Spectrum Disorders (Described Separately)
Dominant Motor and Varying Mental Delay
Cerebral Palsies
Natural History of Cerebral Palsy
Motor Delay Alone
3:
Congenital Malformations of the Brain
INTRODUCTION
INCIDENCE
ETIOLOGY
CLASSIFICATION
Disorder of Neurulation
Cephalocele
Anencephaly
Midline Malformation of the Forebrain
Holoprosencephaly
Agenesis of Corpus Callosum
Corpus Callosum Lipoma
Septo-optic Dysplasia
Arrhinencephaly
Disorder of Neuronal Migration
Clinical Features
Disorder of Cerebellar Development
Cerebellar Aplasia
Joubert's Syndrome
Chiari Malformation
Types
Clinical Features
Dandy-Walker Malformation
Hypertrophic Dysplasia of the Brain
Disorder of Ventricular System
Porencephaly
Hydranencephaly
Aqueductal Stenosis
Arachnoid Cyst
Vascular Malformation
Vein of Galen Malformations
TREATMENT OF CONGENITAL BRAIN MALFORMATIONS
Prevention
4:
Approach to Intracranial Infections in Children
INTRODUCTION
CLINICAL PRESENTATION
INVESTIGATIONS
Cerebrospinal Fluid (Table 2)
SPECIFIC FINDINGS IN MAGNETIC RESONANCE IMAGING
Electroencephalogram
Polymerase Chain Reaction
5:
Clinical Features and Management of CNS Infection in the Child
INTRODUCTION
Infections of Meninges
Parenchymal Infections
Encephalitis and Brain Abscess
BACTERIAL MENINGITIS
Clinical Presentation
Immunologic Defects
Persistent Cerebrospinal Fluid Communications (Recurrent Meningitis)
VIRAL MENINGITIS
TUBERCULOUS MENINGITIS
FUNGAL MENINGITIS
ENCEPHALITIS
BRAIN ABSCESS
INVESTIGATIONS
During Lumbar Puncture
Cerebrospinal Fluid Contamination with Blood
Other Tests
IMAGING STUDIES
TREATMENT
Supportive Measures
Antibiotic Therapy
Neonate
Infant and Children
Anti-inflammatory Treatment
Pediatric Dose
MANAGEMENT OF COMPLICATIONS
Repeated Episodes of Meningitis
PROPHYLAXIS
Vaccines
OTHER MENINGOENCEPHALITIDE
Viral Meningoencephalitis
Presentation of Viral Encephalitis
Signs
Recognition of Different Types of Viral Meningoencephalitis
Investigations
Imaging Studies
Polymerase Chain Reaction and Antibody Detection
Treatment
General Measures
Controlling Increased ICP
Specific Treatment for HSV Meningoencephalitis and VZV Encephalitis
Mortality and Morbidity
Prevention of Viral Meningitis
Pesticides
Japanese Encephalitis Vaccine
6:
Brain Abscess
INTRODUCTION
DIAGNOSIS
Focal Signs
LABORATORY STUDIES
Imaging Studies
Treatment
Antibiotics
Dosage
CURRENT RECOMMENDATIONS
PROGNOSIS
7:
Approach to Childhood Neurotuberculosis
EPIDEMIOLOGY
PATHOGENESIS OF CNS TUBERCULOSIS
CLASSIFICATION OF CNS TUBERCULOSIS
CLINICAL FEATURES OF TUBERCULAR MENINGITIS
Stage 1
Stage 2
Stage 3
Diagnosis
Cerebrospinal Fluid Examination
Immune Based Rapid Blood Tests
Intradermal Tuberculin Skin Test
Imaging
Differential Diagnosis
Tubercular Encephalopathy
Intracranial Tuberculoma
Intracranial Tubercular Abscess
Pott's Spine
Non-osseous Spinal Cord Tuberculosis
Spinal Tubercular Meningitis
Tubercular Arachnoiditis
CENTRAL NERVOUS SYSTEM TUBERCULOSIS IN HIV INFECTED PERSONS
Treatment of CNS Tuberculosis
Antitubercular Treatment Regimens
Drug-resistant Disease
Suggested Drug Regimen for Proved Drug Resistance33
Role of Corticosteroids
Role of Neurosurgery
Prognosis
Prevention
8:
Approach to Cerebral Malaria
CEREBRAL MALARIA
DEFINITION
PATHOPHYSIOLOGY
CLINICAL FEATURES
DIAGNOSIS OF CEREBRAL MALARIA
INVESTIGATIONS
MANAGEMENT
Initial Assessment and Management
Specific Antimalarial Treatment
Artemisinin Derivatives
Dosages
Cinchona Alkaloids
Follow on Treatment
Pre-referral Treatment
Adjunctive Treatment
Continuing Supportive Care
PREVENT RECRUDESCENCE AND TRANSMISSION
PROGNOSIS
9:
Approach to a Child with Neurocysticercosis
WHEN TO SUSPECT NEUROCYSTICERCOSIS?
WHAT ARE THE DIFFERENT TYPES OF NEUROCYSTICERCOSIS?
WHAT ARE THE DIFFERENT STAGES OF THE CYSTICERCUS CYST?
HOW TO CONFIRM THE DIAGNOSIS OF NEUROCYSTICERCOSIS?
Computed Tomography
Magnetic Resonance Imaging
Magnetic Resonance Spectroscopy Scan
Serological Tests
Other Tests
HOW TO DIFFERENTIATE BETWEEN TUBERCULOMA AND NEUROCYSTICERCOSIS?
HOW TO TREAT NEUROCYSTICERCOSIS?
How to Treat Seizures in Neurocysticercosis?
Should the Cysticidal be Used?
Should the Steroids be Used?
Role of Surgery
10:
Approach to Fungal Infection of Central Nervous System
INTRODUCTION
ETIOLOGY
EPIDEMIOLOGY AND RISK FACTORS
PATHOGENESIS
CLINICAL SYNDROMES
DIAGNOSIS
DEFINITIVE TESTS
TREATMENT
Drugs
Specific Treatment
11:
Approach to a Child with Reduced Sensorium
HOW TO ASSESS AND STABILIZE?
REVIEWING THE HISTORY
PERFORMING FOCUSED CLINICAL EXAMINATION
CONDUCTING RELEVANT DIAGNOSTIC TESTS
Neuroimaging
Electroencephalography
Cerebrospinal Fluid Examination
Tests for Inborn Errors of Metabolism
Toxicology Screen
Other Tests
PREFERRED TERMINOLOGY
12:
Anatomy and Localization of Neurological Disorders
INTRODUCTION
ANATOMY
Meninges and Intervening Spaces
BRAIN
LIMBIC SYSTEM
SUBCORTICAL STRUCTURES
Gray versus White Matter
Diencephalon
Brainstem and Cranial Nerves
Anteroposterior Brainstem Anatomy
Rostrocaudal Brainstem Anatomy
Cranial Nerves
Cerebellum
SPINAL CORD
LOCALIZATION OF NEUROLOGICAL LESION
Lower Motor Neuron Localization
Spinal Cord Lesions
Lower Motor Neuron Weakness
13:
Approach to Acute Stroke Syndromes
INTRODUCTION
DEFINITION
ARTERIAL ISCHEMIC STROKES
Risk Factors and Etiology
Cardiac Disorders
Hematological Conditions
Arteriopathies
Arterial Dissection
Moyamoya Pattern
Clinical Presentation
Diagnosis
Acute Management
Long-term Management
VENOUS SINUS THROMBOSIS
HEMORRHAGIC STROKES
Etiology
Clinical Presentation
Diagnosis
14:
Febrile Seizures
INTRODUCTION
DEFINITION
CLASSIFICATION OF FEBRILE SEIZURES
Simple Febrile Seizures
Complex Febrile Seizures
Febrile Status Epilepticus
ETIOLOGY: GENETIC BASIS AND RISK FACTORS
Risk Factors for First Febrile Seizure
APPROACH TO A CHILD WITH FEBRILE SEIZURES
History
Examination
Differential Diagnosis
Investigations
Lumbar Puncture
Electroencephalogram and Neuroimaging
Treatment
Treatment of Acute Attack of Seizures
Parental Counseling
Emergency Management at Home
Prophylaxis
Major Predictors for Recurrent Febrile Seizures
Types of Prophylaxis
Guidelines for Long-term Management
PROGNOSIS
Risk Factors for Epilepsy in Children with Febrile Seizures
CONCLUSION
15:
Approach to a Child with Epilepsy
INTRODUCTION
DEFINITION
First Step
Second Step
Third Step
Physical and Systemic Examination
Fourth Step
Fifth Step
Sixth Step
Managing Comorbidities in Childhood Epilepsy
Seventh Step
Investigations
Eighth Step
Ninth Step
16:
Approach to Benign Epilepsy Syndromes
INTRODUCTION
BENIGN CHILDHOOD EPILEPSY WITH CENTROTEMPORAL SPIKES
Clinical Manifestations
Electroencephalogram Manifestations
Investigations
Treatment
Prognosis
BENIGN OCCIPITAL EPILEPSY WITH PANAYIOTOPOULOS SYNDROME
Clinical Manifestations
Electroencephalography Manifestations
Treatment
Prognosis
IDIOPATHIC CHILDHOOD OCCIPITAL EPILEPSY (GASTAUT)
Clinical Manifestations
Electroencephalography Manifestations
Treatment and Prognosis
BENIGN PARTIAL EPILEPSY OF INFANCY
BENIGN PARTIAL EPILEPSY WITH AFFECTIVE SYMPTOMS
SUMMARY
17:
Approach to Intractable Epilepsy in Children
DEFINITION
FACTORS DETERMINING INTRACTABLE EPILEPSY
MECHANISM OF DRUG RESISTANCE
MANAGEMENT OF REFRACTORY EPILEPSY
ANTIEPILEPTIC DRUGS
KETOGENIC DIET
EPILEPSY SURGERY
CONCLUSION
18:
Seizure Mimics in Infancy and Childhood
NONEPILEPTIC ATTACK DISORDERS OF CHILDHOOD
NEONATAL SEIZURE MIMICS
Jitteriness
Benign Neonatal Sleep Myoclonus
INFANTILE MIMICS
Breath-holding Spells or Reflex Anoxic Seizure
Incidence
Clinical Features
Diagnosis
Management
PAROXYSMAL TORTICOLLIS
Etiology
Clinical Features
Management
BENIGN PAROXYSMAL VERTIGO
Etiology
Clinical Features
Management
MYOCLONUS OF INFANCY
Clinical Features
Diagnosis
Management and Prognosis
HYPEREKPLEXIA
Clinical Diagnosis
Diagnosis
Genetic Testing
Management
Prognosis
SHUDDERING ATTACKS
Clinical History
Diagnosis
Treatment
Prognosis
ALTERNATING HEMIPLEGIA OF CHILDHOOD
Clinical Features
Etiology
Diagnosis
Management
Prognosis
CYCLIC VOMITING SYNDROME
Pathophysiology
Clinical Features
Supportive Criteria
Precipitating Events
Laboratory Studies
Treatment
MIGRAINE
Migraine Variants
Hemiplegic Migraine
Confusional Migraine
Abdominal Migraine
Basilar Migraine
Migraine Aura without Headache
Benign Paroxysmal Vertigo of Childhood
Ophthalmologic Migraine
Causes
Laboratory Studies
Indication of Neuroimaging in Children with Headache
Treatment
Medical Care
Prophylaxis
Treatment of Status Migrainosus
Emergency Department Treatment
Inpatient Treatment
PSYCHOGENIC NONEPILEPTIC SEIZURE
Causes
Clinical Presentation
Diagnosis
Video Electroencephalography Monitoring
Management
Prognosis
SYNCOPE
COMMON CONDITIONS OF SYNCOPE
Evaluation
Investigations
Treatment
TICS
DSM 4 Diagnostic Criteria for Tourette's Disorder
Management
Behavioral Treatment
Pharmacologic Intervention
OPSOCLONUS
Opsoclonus Myoclonus Syndrome
Signs and Symptoms
Diagnosis
Treatment
SPASMUS NUTANS
GASTROESOPHAGEAL REFLUX
JACTATIO CAPITIS
MASTURBATION
19:
Approach to Neonatal Seizures
INTRODUCTION
EPIDEMIOLOGY/INCIDENCE
DEFINITION
PATHOPHYSIOLOGY
Why is the Neonatal Brain More Susceptible to Seizures?
Why Do Neonatal Seizures Present Differently?
Brain Injury in Neonatal Seizures
CLASSIFICATION OF NEONATAL SEIZURES
Subtle Seizures
Focal Clonic Seizures
Multifocal Clonic Seizures
Tonic Seizures
Myoclonic Seizures
RELATION OF SEIZURE TO ELECTROENCEPHALOGRAPH
Does Absence of EEG Seizure Activity Indicate that a Clinical Seizure is Nonepileptic?
DIFFERENTIAL DIAGNOSIS
Seizure Mimic—Normal Activity during Awake or Drowsy State
Sleep
Jitteriness versus Seizure (Table 1)
Apnea: Epileptic versus Nonepileptic
Benign Neonatal Sleep Myoclonus
ETIOLOGY OF NEONATAL SEIZURES
Etiology in Relation to Time of Seizure Onset and Frequency
Hypoxic-Ischemic Encephalopathy
Hypoglycemia
Others
IDIOPATHIC SYNDROMES OF CLINICAL SEIZURES IN THE NEWBORN
Epileptic Syndromes
Nonepileptic Syndromes
Benign Familial Neonatal Seizures
Benign Idiopathic Neonatal Seizures—5th Day Fits
Early Myoclonic Encephalopathy
Early Infantile Epileptic Encephalopathy (Ohtahara Syndrome)
APPROACH TO NEONATAL SEIZURES
Investigations
MANAGEMENT OF NEONATAL SEIZURES (TABLE 2)
Role of Newer Antiepileptic Drugs
Maintenance Therapy
How Does One Assess the Adequacy of Treatment?
Determinants of Duration of Therapy of Anticonvulsant Drugs (Box 3)
PROGNOSIS (TABLE 3)
Risk of Recurrence
Risk of Subsequent Epilepsy: 10–30%
PREVENTION OF NEONATAL SEIZURES
LONG-TERM OUTCOME
20:
Practical Approach in Management of Status Epilepticus
INTRODUCTION
DEFINITION
OUTCOME OF STATUS EPILEPTICUS
MORBIDITY AND MORTALITY ?
CLASSIFICATION OF STATUS EPILEPTICUS
ETIOLOGY
CAUSES
DRUGS WHICH CAN CAUSE SEIZURES
HEMODYNAMICS
PATHOPHYSIOLOGY
MANAGEMENT GOALS
SUPPORTIVE CARE
ANTICONVULSANTS
TREATMENT
Drug Therapy
RAPID-ACTING ANTICONVULSANTS
Pharmacology
Midazolam
Lorazepam
Diazepam
Stage 1 (0 minute)
Stage 2 (5 minutes)
Stage 3 (10 minutes)
Stage 4 (45 minutes)
Stage 5 (60 minutes)
Other Options
TREATMENT OF REFRACTORY STATUS EPILEPTICUS
TREATMENT OF STATUS EPILEPTICUS: WHAT NOW?
NONINTRAVENOUS STATUS EPILEPTICUS
MANAGEMENT AFTER STOPPING OF CONVULSIONS
COMPLICATIONS
SUMMARY
21:
Approach to Neurophysiology Investigations
INTRODUCTION
ELECTROENCEPHALOGRAPHY (EEG)
Clinical Use
Method
Wave Patterns
Frequency
Delta Waves
Theta Waves
Alpha Waves
Beta Waves
Amplitude
Recording of the Electroencephalography
ELECTRODES AND THEIR APPLICATION
Scalp EEG Electrodes
Electrode Placement: The 10–20 System
Organizing and Viewing EEG Activity: The Montage
Recording Requirements and Safety
Technical Requirements for EEG Recordings
Electrical Safety
WEST SYNDROME (FIGS 10 AND 11)
Classical Hypsarrhythmia on EEG (Fig. 12)
Early Childhood
LENNOX-GASTAUT SYNDROME
Electroencephalography (Fig. 14)
MYOCLONIC ASTATIC
Electroencephalography
CHILDHOOD ABSENCE
Electroencephalography (Figs 17 and 18)
SYNDROMES IN ADOLESCENCE (FIGS 19 TO 22)
Photosensitive Epilepsy
Partial-onset Seizures (Fig. 23)
Generalized-onset Seizures (Figs 24 and 25)
ELECTROMYOGRAPHY AND NERVE CONDUCTION VELOCITY
Nerve Conduction Study/Needle EMG Test
What Type of Patient Needs an NCV/EMG?
What Types of Conditions are Diagnosed with NCV/EMG?
How Do I Prepare for an Electromyogram?
How is the Test Performed?
What is an EMG/NCV Test?
NERVE CONDUCTION STUDY
Motor Nerve Conduction (Fig. 28)
Sensory Nerve Conduction (Fig. 29)
Electromyography
Electromyography Needle Electrodes
Recording Technique
ELECTRONYSTAGMOGRAPHY SUMMARY
EVOKED POTENTIALS
Evoked Potential
General Techniques
Evoked Potential Modalities
VISUAL EVOKED POTENTIALS
Stimulus
Pattern-Reversal VEP
Flash VEP
Recording Technique
Response
Interpretation
Disorders
BRAINSTEM AUDITORY EVOKED POTENTIAL
Interpretation
Disorders
Acoustic Neuroma
Multiple Sclerosis
Brainstem Stroke
Brainstem Tumor
Coma
Brain Death
Premature Infants
Neonatal Hypoxia
22:
Basics of MRI and CT
INTRODUCTION
COMPUTED TOMOGRAPHY
Spiral CT
Clinical Application of Spiral CT
Vascular Studies
General Surveys
Pediatric Studies
MAGNETIC RESONANCE IMAGING
Proton Density
T1 and T2 Weighted Images
Magnetic Resonance Angiography
Pulse Sequences/Image Plan
RECENT ADVANCES IN MRI
Functional MRI (fMRI)
Cerebral Blood Flow Imaging
Diffusion Imaging
Perfusion Imaging
Magnetic Resonance Spectroscopy
CT AND MRI TECHNIQUES
MRI TECHNIQUES
Normal axial CT and MRI Scan Anatomy
Above foramen Magnum Level
Level of the Fourth Ventricle
Third Ventricular
Ventricular Level
SOME NEUROIMAGING FEATURES
Posterior Fossa Mass—Child
Cerebellum/Fourth Ventricle
Intraventricular Tumor
Tuberculosis
CT Findings
Cysticercosis
CT Findings
SOME COMPARATIVE SCANS (Figs 10 to 15)
23:
Guidelines for the Diagnosis and Management of Childhood Epilepsy
INTRODUCTION
OBJECTIVES
RECOMMENDATIONS
Neonatal Seizures
Acute Symptomatic Seizures
Febrile Seizures
Granuloma in Children
Idiopathic Partial Epilepsies in Childhood
Benign Epilepsy with Centrotemporal Spikes (Benign Rolandic Epilepsy)
Panayiotopoulos Syndrome (Early-Onset Childhood Epilepsy with Occipital Paroxysms)
Idiopathic Generalized Epilepsies
Childhood Absence Epilepsy (Petit-mal)
Idiopathic Generalized Epilepsies of Adolescence
Investigations for Epilepsy
Electroencephalography
Neuroimaging
Management of First Unprovoked Seizure
Management of Newly Diagnosed Epilepsy
Severe Epilepsy Syndromes of Early Childhood/Epileptic Encephalopathies (Catastrophic Epilepsies in Infancy and Early Childhood)
West Syndrome
Lennox-Gastaut Syndrome
Dravet Syndrome (Severe Myoclonic Epilepsy of Infancy)
Refractory Epilepsies in Older Children and Adolescents
Mesial Temporal Lobe Epilepsy
Epilepsia Partialis Continua
Epilepsies and Cognition
Antiepileptic Drugs
Phenobarbitone
Phenytoin
Fosphenytoin
Valproate
Carbamazepine
Oxcarbazepine
Clobazam
Clonazepam
Lamotrigine
Levetiracetam
Topiramate
Zonisamide
Lacosamide
Rufinamide
Stiripentol
Tiagabine
Drug Resistant Epilepsy
Nonpharmacological Treatment
Ketogenic Diet and Modified Atkins Diet in Epilepsy
Surgical Treatment
STATUS EPILEPTICUS
24:
Approach to a Child with Cerebral Palsy
INTRODUCTION
Does this Child Have Cerebral Palsy?
What Type of Cerebral Palsy is this?
Could it be a Progressive or Treatable Neurological Disorder Rather than Cerebral Palsy?
What is the Functional Status of the Child?
Does this Child have any Other Comorbidity Associated with Cerebral Palsy?
Does this Child Need Medicines?
Could any Multidisciplinary Support/ Surgical Intervention Help?
Can Stem Cell Therapy Help?
25:
Approach to Autism Spectrum Disorders
INTRODUCTION
AUTISM FEATURES
AUTISM
Definition
PERVASIVE DEVELOPMENTAL DISORDER (DSM IV)
CRITERIA FOR AUTISTIC DISORDER (DSM IV)
Triad of Autism
A Total of Six or More Manifestations from One to Three
COMMUNICATION DEFICITS IN AUTISM
AUTISM: PLAY
COGNITIVE DYSFUNCTION IN AUTISM
SENSORIMOTOR SYMPTOMS IN AUTISM
INSTRUMENTS FOR DIAGNOSIS OF ASD
EARLY RECOGNITION
MANAGEMENT
AUTISM: DIFFERENTIAL DIAGNOSES
CHILDHOOD DISINTEGRATIVE DISORDER (HELLER DEMENTIA)
Rett Syndrome
26:
Approach to Neurodegenerative Disorders in Children
NEURODEGENERATIVE DISORDERS
WHEN TO SUSPECT THAT THERE IS NEURODEGENERATION?
Approach
Step I: Is it Progressive or Static?
Step II: Find Out Site/Sites of Affection
Pure motor regression:
Step III: Rule Out Other Treatable Conditions
When to suspect degenerative/metabolic diseases?:
WHAT TO LOOK FOR IN THE EXAMINATION?
Formulating the Diagnosis
Nonprogressive Central Motor Disorder (CP)
Progressive Central Disorder
Peripheral Progressive Disorder
Investigations
Myoclonus Ataxia Dementia Syndrome
Progressive Epstein Syndrome
Prognosis
27:
Movement Disorders
INTRODUCTION
Differences from Epilepsy1
APPROACH TO DIAGNOSIS
Self-injurious Behavior3
Drug-induced Movement Disorders4
Genetics in Movement Disorders5
ODD MOVEMENT DISORDERS6
MANAGEMENT
Summary of Drugs used in Movement Disorders
28:
Approach to a Child with Opsoclonus-Myoclonus Syndrome
INTRODUCTION
HISTORICAL NOTE
INCIDENCE AND ASSOCIATIONS
CLINICAL FEATURES
Opsoclonus
Myoclonus
Ataxia
Encephalopathy or Behavioral Change
INVESTIGATIONS
PATHOGENESIS
MANAGEMENT
OUTCOME
PRACTICE POINTS
29:
Ataxia in Children
INTRODUCTION
ETIOLOGY
Causes of Acute Ataxia
Subacute Ataxia
Episodic/Recurrent Ataxia
Chronic Ataxia
CERTAIN TYPES OF CEREBELLAR ATAXIA
Chronic Nonprogressive/Slowly Progressive
Autosomal Recessive Hereditary Ataxias
Autosomal Dominant Cerebellar Ataxias (ADCA)
X-linked Ataxias
Symptomatic Ataxias
A SPECIAL SYNDROME: JOUBERT SYNDROME
INVESTIGATION
TREATMENT
30:
Approach to Neuromuscular Diseases in Children
APPROACH TO DIAGNOSIS
FLOPPY INFANT
INVESTIGATIONS
POINTS TO LOOK FOR IN PHYSICAL EXAMINATION
INVESTIGATIONS
31:
Approach to a Floppy Baby
INTRODUCTION
CLINICAL PRESENTATION AND APPEARANCE
DIAGNOSTIC APPROACH
INVESTIGATIONS
THERAPEUTIC APPROACH
32:
Approach to a Child with Myopathy or Myositis
INTRODUCTION
CONGENITAL MYOPATHIES
Classification
Clinical Presentation
Investigations
Treatment
MUSCULAR DYSTROPHIES
Duchenne Muscular Dystrophy (DMD)
Clinical Presentation
Investigations
Treatment
Genetic Counseling
Myotonic Muscular Dystrophy
INFLAMMATORY MYOPATHIES
Inflammatory Myopathy Associated with Infection
Influenza Myositis
Dermatomyositis
Clinical Presentation
METABOLIC MYOPATHIES
Pathophysiology
Age of Presentation
Clinical Presentation
Investigations
CHANNELOPATHIES
Classification
Clinical Presentation
33:
Pediatric Headache
MANAGEMENT PROTOCOL
COMPREHENSIVE HEADACHE EXAMINATION
EXAMINATION
INVESTIGATION
IMAGING
Recommendations for Neuroimaging
EEG in Headache
EEG becomes Important
TREATMENT
Primary Headache
During Interval Phase
During Acute Phase
Treatment of Migraine
Acute Treatments for Migraines
Drugs Used in Acute Attack
Triptans
Drugs Used for Prophylaxis
Other Measures
Protocol
Tension Headache
Cluster Headache
Prophylaxis
Chronic Daily Headaches
Treatment for Chronic Daily Headache
Status Migrainosus
Comment
Status Migrainosus Raskin Protocol
AMERICAN ACADEMY OF NEUROLOGY: GUIDELINES
AMERICAN ACADEMY OF NEUROLOGY: PROPHYLAXIS
DRUGS
Propranolol
Amitriptyline
Flunarizine
Imipramine
Cyproheptadine
Divalproex Sodium
Topiramate
Nimodipine
34:
Approach to a Child with Neurocutaneous Syndrome
INTRODUCTION
NEUROFIBROMATOSIS TYPE 1
Clinical Features and Diagnosis
Investigations
Management
NEUROFIBROMATOSIS TYPE 2
Clinical Features and Diagnosis
Investigations
Management
TUBEROUS SCLEROSIS COMPLEX
Clinical Features and Diagnosis
Major Features
Minor Features
Investigations
Management
Sturge-Weber Syndrome
Clinical Features and Diagnosis
Investigations
Management
ATAXIA TELANGIECTASIA
Clinical Features and Diagnosis
Investigations
Management
VON HIPPEL-LINDAU SYNDROME
Clinical Features and Diagnosis
Investigations
Management
35:
Approach to Nutritional Disorders of Nervous System
INTRODUCTION
PROTEIN-CALORIE MALNUTRITION
COBALAMIN (VITAMIN B12)
Clinical Manifestations
Laboratory Findings
Treatment
FOLATE DEFICIENCY
Laboratory Findings
Treatment
THIAMINE
Clinical Manifestations
Treatment
NIACIN
Clinical Manifestations
Treatment
PYRIDOXINE
Clinical Manifestations
VITAMIN E
Clinical Manifestations
Laboratory Findings
Treatment
VITAMIN A AND D
COPPER DEFICIENCY
36:
Approach to Rabies
INTRODUCTION
EPIDEMIOLOGY
Reservoir of Infection
Mode of Transmission
ETIOPATHOLOGY
CENTRAL NERVOUS SYSTEM INVOLVEMENT
CLINICAL FEATURES
DECISION TO TREAT
Vaccination Status of the Biting Animal
Provoked versus Unprovoked Bites
Observation of Biting Animal
Bite by Wild Animals
Bite by Rodents
Bat Rabies
Special Circumstances
Post-exposure Prophylaxis of Immunocompromized Patients
Human-to-Human Transmission
APPROACH TO POST-EXPOSURE PROPHYLAXIS
Management of Animal Bite Wound (Figs 4A to D)
Wound Toilet
Application of Antiseptics
Don'ts
Local Infiltration of Rabies Immunoglobulins
RABIES IMMUNOGLOBULINS
Dose of Rabies Immunoglobulins
Administration of Immunoglobulins
Sensitivity Test before Administration of Equine Rabies Immunoglobulin
Approach to a Patient Requiring Rabies Immunoglobulin When None is Available
ANTIRABIES VACCINES
Indications
Reconstitution and Storage
Adverse Effects with Cell Culture Vaccines
Switch Over from One Brand or Type of Vaccine to the Other
Protective Level of Antirabies Antibody
Intramuscular Regimen
Intradermal Regimens
Concept of Intradermal Inoculation of Antirabies Vaccines
General Guidelines for Use of Intradermal Inoculation of Antirabies Vaccines
VACCINES AND REGIMEN APPROVED FOR INTRADERMAL USE IN THE COUNTRY
Regimen
Updated Thai Red Cross Schedule (2-2-2-0-2)
Intradermal Injection Technique
POST-EXPOSURE PROPHYLAXIS FOR PREVIOUSLY VACCINATED PERSONS
Managing Re-exposure Following Post-exposure Treatment with TCV
Managing Exposure Following Pre-exposure Prophylaxis with TCV
Managing Re-exposure Following Post-exposure Treatment with Nervous Tissue Vaccine
PRE-EXPOSURE VACCINATION
TREATMENT OF CLINICAL RABIES
37:
Neurotoxic Snake Envenomation
INTRODUCTION
MECHANISM OF NEUROTOXICITY
CLINICAL FEATURES
SYSTEMIC ENVENOMATION
MANAGEMENT
FIRST AID
INITIAL TREATMENT
NEUROTOXICITY HAS SET IN—NOW WHAT?
Specific Treatment
Neutralization of Venom
ANTI-SNAKE VENOM: WHEN TO GIVE?
ANTI-SNAKE VENOM: HOW MUCH?
ANTI-SNAKE VENOM ANAPHYLAXIS: WHAT TO DO?
Reversal of Neurotoxicity
Mechanical Ventilation: Anti-snake Venom Ineffective or not Available: What to do?
ANCILLARY TREATMENT
38:
Cerebrospinal Fluid
WHAT DOES THE CEREBROSPINAL FLUID DO?
SOME CEREBROSPINAL FLUID FACTS
BLOOD-BRAIN BARRIER
Lumbar Puncture
Procedure
Contraindications for Performing Lumbar Puncture
CISTERNAL PUNCTURE
Diagnosis made by Lumbar Puncture
ANALYZING CEREBROSPINAL FLUID
POINTS TO REMEMBER
39:
Fundus Examination in Children
INTRODUCTION
Method
Normal Fundus
Macula
Retinal Vessels
Fundus Appearance
PATHOLOGIES
CAUSES OF CHERRY-RED SPOT
Central Retinal Artery Occlusion with Systemic Conditions
RETINOPATHY OF PREMATURITY
HEREDITARY VITREORETINOPATHIES
Differential Diagnosis of Hereditary Vitreoretinopathies
Causes of Retinal Hemorrhage in Infant
Hemoglobinopathies
Retinitis Pigmentosa
Macular Dystrophies
Degenerative Myopia
Purtscher's Retinopathy
Terson's Syndrome
FUNDUS PICTURE APPEARANCES OF SOME IMPORTANT OCULAR DISEASES (FIGS 1 TO 13)
Drugs Appendix
ACETAZOLAMIDE
ACYCLOVIR
ADRENOCORTICOTROPIC HORMONE
ARIPIPRAZOLE
BACLOFEN
BENZATROPINE (BENZTROPINE)
BOTOX (BOTULINUM TOXIN TYPE A)
CARBAMAZEPINE
CARNITINE (LEVOCARNITINE)
CLONAZEPAM
CLONIDINE
CLOZAPINE
CO-CARELDOPA
DANTROLENE
DIAZEPAM
ETHOSUXIMIDE
FELBAMATE
HALOPERIDOL
IMMUNOGLOBULIN (INTRAVENOUS)
LAMOTRIGINE
LEVETIRACETAM
MANNITOL
METHYLPREDNISOLONE
MIDAZOLAM
OLANZAPINE
OXCARBAZEPINE
PENICILLAMINE
PHENOBARBITONE (PHENOBARBITAL)
PHENYTOIN
PIMOZIDE
PIRACETAM
PRIMIDONE
PROPRANOLOL
PYRIDOXINE (VITAMIN B6)
RISPERIDONE
THIAMINE (VITAMIN B1)
TOPIRAMATE
TRICLOFOS SODIUM
TRIENTINE DIHYFROCHLORIDE
TRIHEXYPHENIDYL (BENZHEXOL)
VALPROIC ACID (SODIUM VALPROATE)
VIGABATRIN
ZONISAMIDE
INDEX
TOC
Index
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