PEDIATRIC NEUROLOGY/CHILD NEUROLOGY
Pediatric neurology or child neurology refers to a specialized branch of medicine that deals with the diagnosis and management of neurological conditions in neonates (newborns), infants, children and adolescents. The discipline encompasses diseases and disorders of the spinal cord, brain, peripheral nervous system, autonomic nervous system, muscles and blood vessels that affect individuals in these age groups.
- Acquired Torticollis
- Acute Cerebellar Ataxia
- Acute CNS Demyelination
- Acute Disseminated Encephalomyelitis
- Acute Migraine
- Acute Stroke in Sickle Cell Disease
- Acute Toxic-metabolic Encephalopathy
- Acute Viral Encephalitis
- ADHD
- Adrenoleukodystrophy
- Alexander Disease
- Anencephaly
- AntiseizureDrugs
- Asperger Syndrome
- Ataxia-telangiectasia
- Autism
- Autism Spectrum Disorder
- Batten Disease
- Benign Focal Epilepsies
- Brachial Plexus Injuries
- Brachial Plexus Syndromes
- Bradykinetic Movement Disorders
- Brain Death
- Cerebral Palsy
- Cerebral Venous Thrombosis
- CerebrotendinousXanthomatosis
- Cerebrovascular Disease
- Chiari Malformations
- Child Abuse
- Childhood Absence Epilepsy
- Closed Spinal Dysraphism
- Cold Stimulus Headache
- Coma in Children
- Congenital Muscular Torticollis
- Congenital Myopathies
- Convulsive Status Epilepticus
- Craniosynostosis
- Cyclic Vomiting Syndrome
- Demyelinating Disease
- Developmental and Behavioral
- Developmental/Behavioral Problems
- DravetSyndrome
- Duchenne & Becker Muscular Dystrophy
- Elevated Intracranial Pressure
- Emery-Dreifuss Muscular Dystrophy
- Encephalocele
- Encephalopathy
- Encephalopathy
- Energy Metabolism in Muscle
- Epilepsy
- Epilepsy Syndromes
- Fabry disease
- Facial Nerve Palsy
- Facioscapulohumeral Muscular Dystrophy
- Febrile Seizures
- Fourth Cranial Nerve Palsy
- Friedreich Ataxia
- Gene Therapy for Childhood Neurological Disease
- Genetic Disorders
- Genetic Disorders
- Genodermatoses
- Guillain-Barré Syndrome
- Headache
- Hemorrhagic Stroke
- Hereditary Ataxias
- Hereditary Hemorrhagic Telangiectasia
- Hereditary Neuropathies
- Hereditary Primary Motor Sensory Neuropathies
- Hereditary Sensory & Autonomic Neuropathies
- Hereditary Spastic Paraplegia
- Horner Syndrome
- Huntington Disease
- Hydrocephalus
- Hyperkinetic Movement Disorders
- Hypotonia
- Hypotonia and Weakness
- Idiopathic Intracranial Hypertension
- Infantile Spasms
- Infections
- Intellectual Disability
- Intracranial Epidural Hematoma
- Intracranial Subdural Hematoma
- Intraventricular Hemorrhage
- Ischemic Stroke
- Juvenile Dermatomyositis and Polymyositis
- Juvenile Myoclonic Epilepsy
- Ketogenic Diet
- Krabbe Disease
- Limb-girdle Muscular Dystrophy
- Localization-related Epilepsy
- Lumbar Puncture
- Malformations
- Metabolic Myopathies
- Metachromatic Leukodystrophy
- Migraine with Brainstem Aura (basilar-type migraine)
- Minor Head Trauma
- Mitochondrial Myopathies
- Movement Disorders
- Moyamoya Disease
- Mucopolysaccharidoses
- Multiple Sclerosis
- Muscular Dystrophies
- Muscular Dystrophy
- Myasthenia Gravis
- Myelomeningocele
- Myopathies Affecting Extraocular Muscles
- Myotonic Dystrophy
- Neonatal Brachial Plexus Palsy
- Neonatal Encephalopathy
- Neonatal Epilepsy Syndromes
- Neonatal Neurology
- Neonatal Seizures
- NeurocutaneousDisorders
- Neurofibromatosis
- Neurofibromatosis type 1 (NF1)
- Neuroimaging
- Neuromuscular Disorders
- Neuromuscular Junction Disorders
- NeuromyelitisOptica Spectrum Disorders
- Neuropathies Associated with Hereditary Disorder
- Neuropathy
- Niemann-Pick Disease
- NonepilepticParoxysmal Disorders
- Oculopharyngeal, Distal, and Congenital Muscular Dystrophies
- Ophthalmology
- Optic Neuritis
- Organic Acidemias
- Pediatric Stroke
- Pelizaeus-Merzbacher Disease
- PendularNystagmus
- Peripheral Neuropathies
- Periventricular Leukomalacia
- Peroxisomal Disorders
- Pneumococcal Meningitis
- Primary Motor Stereotypies
- PseudotumorCerebri
- Rett Syndrome
- Rocky Mountain Spotted Fever
- Sagittal Synostosis
- Seizures
- Seizures and Epilepsy
- Sixth Cranial Nerve Palsy
- Sjögren-Larsson Syndrome
- Specific Learning Disabilities
- Spina Bifida
- Spinal Muscular Atrophy
- Spinocerebellar Ataxias
- Status Epilepticus
- Stroke
- Stroke in Children
- Stupor and Coma
- Sturge-Weber
- Sturge-Weber Syndrome
- SupranuclearDisorders of Gaze
- Sydenham Chorea
- Tension-type Headache
- Third Cranial Nerve Palsy
- Tourette Syndrome
- Trauma
- Tuberous Sclerosis Complex
- Urinary Tract Complications of Myelomeningocele
- VagusNerve Stimulation
- Vanishing White Matter Disease
- Vascular Malformations
- Vestibular Migraine
- Viral Meningitis
- Wilson Disease