Differential (Click to cross reference) abdominal distention abducens nerve paralysis acanthocytosis acetazolamide achondroplasia acromicria adverse drug reaction alcohol alcohol, neurologic complications with algorithm alopecia alpha-fetoprotein alveolar hypoventilation amenorrhea aminoacidopathies aminoacidurias ammonia amniocentesis amphetamines anatomy of anemia Angelman syndrome angiokeratoma anorexia nervosa anticonvulsants aphasia apraxia of eye movements aqueduct of Sylvius, stenosis aqueductal stenosis areflexia arthralgia arthritis arylsulfatase B asymptomatic ataxia ataxia telangiectasia ataxia, cerebellar ataxia, progressive ataxia, truncal ataxic gait atlanto-axial subluxation atrial enlargement attention deficit disorder with hyperactivity autism autoimmune disease basal ganglia, calcification of basal ganglia, lesion, bilateral basilar impression Bassen-Kornzweig syndrome battered child syndrome behavior modification behavior, combative behavioral disorder biologic markers bitemporal visual field defect blepharophimosis blepharospasm blind spot, enlarged blindness blindness, sudden bone age bone biopsy bone marrow transplantation brachial plexus neuropathy brachial plexus neuropathy, familial brain atrophy brain biopsy brainstem, atrophy breech delivery bruxism cachexia calcification, gyral calcification, intracranial carbonic anhydrase II deficiency carcinoembryonic antigen carcinoma cardiomyopathy caries CAT scan CAT scan, abnormal CAT scan, false negative cataracts cavernous sinus cavernous sinus, metastasis to celiac disease, adult celiac disease, childhood central hypoventilation, congenital cerebellar ataxia, children cerebellar ataxia, hereditary cerebellar ataxia, primary cerebellar atrophy, secondary cerebellar degeneration cerebral cortex cerebral cortical atrophy cerebral embolism cerebral palsy cerebral vasculature cerebrospinal fluid, biochemical markers of CNS tumors cerebrospinal fluid, cytology cerebrospinal fluid, elevated protein of cerebrospinal fluid, lactic acid concentration cerebrospinal fluid, pressure increased cerebrovascular accident cerebrovascular accident, familial occurrence cerebrovascular accident, infancy and childhood cerebrovascular accident, mimics cerebrovascular accident, multiple cerebrovascular accident, recurrent cerebrovascular accident, young adult chemotherapy, CNS treatment and complications with child abuse children chorea choreoathetosis chorionic gonadotropin chorioretinitis chromosomal abnormality chromosome 11 chromosome 14 chromosome 15 chromosome 8 chronic graft versus host disease chronic progressive external ophthalmoplegia cisterna magna, enlarged cisternogram, radionuclide cleft palate Clinical Pathologic Conference(C.P.C.) clinodactyly Cockayne's syndrome codfish vertebrae cold hands sign collagen vascular disease coma complications compression fracture congenital heart disease congenital heart disease, CNS complications with congenital malformation congenital malformation, non CNS conjunctivitis consanguinity contractures, joint cornea, abnormal cornea, opacity of Cornelia de Lange syndrome corpus callosotomy corpus callosum, atrophy of corpus callosum, hypoplastic corpus callosum, thinning cortical blindness cranial nerve palsies craniopharyngioma creatine phosphokinase(CPK)elevated cry, abnormal cry, weak cryopyrin-associated periodic syndrome cryptorchidism cultured skin fibroblasts cystinosis cystinuria cytochrome c oxidase cytochrome c oxidase, deficiency deafmute deafness degenerative diseases of CNS dementia dementia, childhood dementia, rapidly progressive dentate nuclei, lesion of dermatitis herpetiformis developmental disability developmental evaluation developmental milestones developmental milestones, loss of developmental retardation diabetes insipidus diabetes mellitus diagnostic criteria diarrhea differential diagnosis difficulty climbing stairs digits, abnormal diplopia dislocated hip, congenital dissociated sensory loss distal muscle atrophy distal muscle weakness dopa responsive dystonia drooling dural sinus thrombosis dwarfism dysarthria dyslexia dysmorphic dysostosis multiplex dysphagia dyspraxia dystonia ear, abnormal ears, low set eating disorder echocardiogram echocardiogram, transesophageal ectopic pinealoma ejection fraction ejection fraction, abnormal electroencephalogram electroencephalogram, abnormalities of electromyogram electron microscopy empty sella encephalopathy encephalopathy, progressive endovascular therapy enophthalmous enzyme treatment enzyme, defect enzyme, muscle disease enzyme, serum epicanthal folds epidemiology of neurology episodic disorders evoked potentials exercise exercise intolerance exome sequencing exostosis eye movement, disorders of eyebrows, abnormal eyes, sunken facial anomalies facial appearance, abnormal facial hypoplasia facial nerve palsy failure to thrive false negative familial fatigue feeding disorder fetal alcohol syndrome fetus fever fever, recurrent fibrillations finger tapping floppy infant foam cells follicle stimulating hormone foot drop foot drop, bilateral fracture, pathologic Friedreich's ataxia frontal bossing fucosidosis gadolinium gait disorder gait, apraxic gait, spastic gangliosidosis GM1 gangliosidosis GM2 gargoylism gastrointestinal disease, neurologic complications gastrointestinal motility gender gene gene mutation genetic counselling genetic diagnosis genetic diagnosis, prenatal genetic linkage genetic neurologic disorders genetic screening genetic testing genital hypoplasia genu valgum glaucoma glucose tolerance test, abnormal gluten ataxia gluten sensitivity gluten-free diet glycogen debranching enzyme deficiency glycogen storage disease glycoprotein Gowers maneuver gray hair growth hormone growth hormone deficiency growth retardation hair, darkening of hair, loss Hallgren's syndrome hamartoma hand flapping hand weakness head circumference head injury head injury, hypothalamic and pituitary damage head injury, pediatric headache headache, recurrent hearing loss heart block heart murmur hemiparesis hemoglobin abnormality, neurologic complications of hemorrhage, intracranial, newborn hemorrhagic diathesis hepatitis hepatomegaly hepatosplenomegaly heralding manifestation hereditary multiple exostoses herpes simplex virus herpes simplex virus infection, newborn herpes simplex virus, human nervous system and high arched palate hip dysplasia Hirschprung's disease hirsutism HLA homocystinuria Hunter's syndrome Hurler's syndrome hydrocephalus hydrocephalus, normal pressure hydrocephalus, normal pressure in children hypercapnia hyperhomocysteinemia hyperphagia hyperpigmentation of skin hyperreflexia hypertelorism hypertonia hypertrophic cardiomyopathy hypertrophic intracranial pachymeningitis hypodontia hypoglycemia hypogonadism hypomagnesemia hypomyelination hypoparathyroidism hypopigmentation of skin hypopituitarism hyporeflexia hypotelorism hypothalamus hypothalamus, disturbance of hypothalamus, lesion of hypothalamus, neoplasm of hypothermia hypothermia, causes of hypothyroidism hypotonia hypotonia, infants hypoxia iatrogenic neurologic disorders imbalance immunodeficiency immunosuppression imperforate anus impulsivity inability to stand on tiptoes inclusion bodies, intranuclear infection, recurrent insulin resistance intellectual deficit intellectual deterioration intelligence quotient intestinal biopsy intestinal pseudoobstruction intracranial hemorrhage intracranial hypertension, benign intracranial hypertension, benign, differential diagnosis intracranial hypertension, benign, pathogenesis of intracranial pressure, increased intrauterine intrauterine infection intrauterine infection, viral joint hypermobility Kearns-Sayre syndrome keratoconus Klinefelter's syndrome Krabbe's disease kyphoscoliosis, neurologic causes of lactate lactic acidemia laminar necrosis, cortical language disorders in children Laurence-Moon-Bardet-Biedl syndrome L-dopa learning disability learning disability, in children Leber's hereditary optic neuropathy leg weakness, bilateral Leigh's disease lens, dislocation of lens, ectopic leukemia leuko-araiosis leukodystrophy leukodystrophy, 4H leukoencephalopathy level of consciousness, decreased lid lid abnormalities life expectancy lip, abnormal lipid storage disorder of CNS livedo reticularis low birth weight Lowe's syndrome lumbar puncture luteinizing hormone lymphoma lysosomal storage disease macrocephaly malabsorption malabsorption syndrome malformation, CNS, congenital megalencephaly melanomatosis, primary malignant MELAS syndrome meningitis, aseptic menses mental retardation mental status, abnormal MERRF syndrome metabolic acidosis metabolic disorder, primary metachromatic leukodystrophy microcephaly micrognathia micromelia microspherophakia migraine misdiagnosis mitochondrial disease mitochondrial encephalomyopathy MNGIE syndrome molecular genetics Morquio syndrome mortality movement disorder movement disorder, extrapyramidal MRI MRI, abnormal MRI, CAT scan compared to MRI, contrast enhanced MRI, diffusion weighted MRI, disappearing lesion on MRS mucopolysaccharidoses multiple system atrophy muscle biopsy muscle cramp muscle spasm muscle stiffness muscle weakness muscle weakness, proximal myasthenia gravis, differential diagnosis myasthenia gravis, misdiagnosis of myelination of nervous system myelopathy myoclonus myoclonus, epilepsy myopathy myopathy, distal myopathy, distal, vacuolar myopathy, inclusion body myopathy, inclusion body, hereditary myopathy, mitochondrial myopathy, vacuolar myopia myotonia nasal bridge, wide nausea and vomiting neck, webbed negative neoplasm, intracranial with metastasis extracranially neoplasm, pituitary neoplasm, primary intracranial-treatment of neoplasm, primary of CNS neoplasm, primary of CNS-children neoplasm, primary of CNS-incidence of neoplasm, primary of CNS-survival neoplasm, primary of CNS-treatment of nerve biopsy neuritis neurocutaneous disease neuroendocrinology neurologic complications of, systemic cancer neurologic complications of, systemic disease neurologic disease neurologic disease, diagnoses of neurologic examination, focal neurologic signs neuroophthalmology neuropathology neuropathology, brain neuropathy neuropathy, peripheral Niemann-Pick disease Noonan Syndrome normal nose, abnormal nystagmus nystagmus, see-saw obesity ocular motility, disorders of ocular myopathy oligodactyly ophthalmoplegia ophthalmoplegia, progressive external optic atrophy optic atrophy, bilateral optic foramina optic foramina, abnormal optic nerve sheath fenestration optic nerve, decompression of optic neuropathy oral ulcerations osteogenesis imperfecta osteopetrosis osteoporosis otosclerosis P300 Pallister-Hall syndrome palpebral fissure, short pancytopenia papilledema paraparesis paraparesis, spastic Parkinson disease, differential diagnosis of Parkinsonism syndrome PAS positive patent ductus arteriosus pathology pectus carinatum pectus excavatum perceptual-motor dysfunction personality change philtrum, hypoplastic philtrum, tented phocomelia photophobia photosensitivity, skin pigmentary retinopathy pinched face pituitary pituitary stalk pituitary, adenoma pituitary, dysfunction pituitary, enlargement pituitary, hyppoplasia pituitary, lesion of PLEDs PLEDs, bilateral independent PLEDs, etiology of pleocytosis of cerebrospinal fluid polydactyly polyhydramnios polyps, gastrointestinal tract posterior pituitary ectopia postural abnormality Prader-Labhart-Willi syndrome precocious puberty pregnancy, neurologic complications in premature infant prenatal diagnosis by amniocentesis pretectal syndrome progeria prognathism prognosis progressive neurologic disorder proteinuria pseudoretinitis pigmentosa psychiatric disorder psychiatric problems in neurologic disorders psychological testing psychological testing, children psychomotor retardation psychosis psychosocial aspects ptosis puberty puberty, delayed pulmonary stenosis pupil, abnormality in neurologic disorders pupil, ectopic-congenital putamen, lesion of putamen, lesion of, bilateral quadriparesis quadriplegia radiation hypersensitivity radiation therapy, CNS treatment and complications with ragged-red fibers rapidly progressing neurologic illness rash reading problem, causes of recurrent red eye renal failure renal tubular acidosis ReNU syndrome respirations in CNS disease respirator respiratory failure respiratory tract infection retinal degeneration retinitis pigmentosa retinopathy Rett's syndrome review article rickets risk factors ritalin rocking root lesion, nerve saddle nose Sanfilippo syndrome schizophrenia Schwartz-Jampel syndrome sclerae, blue scoliosis scoliosis, neurologic association with seizure seizure, children seizure, drug resistance seizure, focal seizure, injury following sella turcica, enlargement of sella turcica, hypoplasia of sensorineural hearing loss serologic testing short neck short stature shunt procedure, lumboperitoneal sickle cell trait simian crease skin, biopsy skin, darkening of skin, lesions in neurologic disorders skull bone, thickening skull x-ray, abnormal skull x-ray, bony defect on sleep sleep pathology and physiology small vessel disease somatosensory evoked potentials spasticity speech disorder speech disorder, childhood speech, absence of speech, delayed development of Spielmeyer Vogt syndrome spinal cord, compression of spinal cord, lesion of spinal muscular atrophy splenomegaly spongy degeneration of brain standing difficulty stem cell transplantation stent, venous sinus steppage gait stereotyped behavior stimulant drugs stooped posture strabismus strokelike episodes subarachnoid hemorrhage subdural hematoma subdural hematoma, neonates and infants suck, poor suprasellar lesion syndactyly synophrys systemic illness teeth, abnormal telangiectases temper tantrums temporal lobe, lesion teratoma third ventricle, mass of thyroid function tests toe walking tongue, enlarged tongue, protrusion of treatment of neurologic disorder tremor tremor, postural tremulousness trichopoliodystrophy upgaze, paralysis of urea-cycle enzymopathies urinary 17 hydroxycorticosteroids urinary 17 ketosteroids Usher's syndrome valvulopathy viral infection, CNS visual acuity, decreased visual field defect visual field testing visual fields, constricted visual impairment visual loss vomiting, recurrent walking, difficulty with weakness weakness, generalized weight gain weight loss Werner's syndrome wheelchair white matter disease whole genome sequencing wide based gait xeroderma pigmentosa x-linked mental retardation x-ray, cervical spine

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