Differential (Click to cross reference) aciduria aggression aminoacidopathies aminoacidurias amyloidosis anemia anemia, megaloblastic aneurysm aneurysm, intracranial aneurysm, intracranial, familial anticoagulant, treatment arachnodactyly areflexia arrhythmia, cardiac atrial myxoma B 12 deficiency B 12 deficiency, infants B 12 metabolism, defective Babinski sign bedridden behavior, combative behavioral disorder brain atrophy breast feeding cardiomyopathy CAT scan, abnormal cavernous hemangioma cerebral embolism cerebral venous thrombosis cerebrospinal fluid, gammaglobulin of cerebrospinal fluid, red cells in cerebrovascular accident cerebrovascular accident, familial occurrence cerebrovascular accident, infancy and childhood cerebrovascular accident, recurrent cerebrovascular accident, young adult cerebrovascular disease cerebrovascular disease, premature children cholelithiasis Clinical Pathologic Conference(C.P.C.) clonus coagulopathy cobalamin C deficiency codfish vertebrae cognition coma confusion consanguinity cortical vein thrombosis cystinuria D-dimer dementia developmental retardation diet dural sinus thrombosis dysmorphic ecchymoses Ehlers-Danlos syndrome electroencephalogram, abnormalities of emotional lability enzyme, defect Fabry's disease facial anomalies facial appearance, abnormal facial hypoplasia familial fibromuscular dysplasia fingers, abnormal frontal bossing gait disorder gene mutation genetic neurologic disorders genetic testing gout headache headache, positional heart murmur hemoglobin abnormality, neurologic complications of heralding manifestation hereditary hemorrhagic telangiectasia(HHT) homocystinuria homocystinuria, heterozygous hydrocephalus hyperhomocysteinemia hyperpigmentation of skin hyperreflexia hypothermia hypotonia hypotonia, infants inappropriate behavior inborn errors of metabolism insulin resistance intellectual deterioration intracerebral hemorrhage intracerebral hemorrhage, young adult kyphoscoliosis, neurologic causes of laughing, pathologic lens, dislocation of lens, ectopic lethargy leukoencephalopathy Lhermitte's sign livedo reticularis malformation, vascular malformation, vascular, cerebral malformation, vascular, familial marfanoid skeletal abnormalities melanomatosis, primary malignant mental status, abnormal metabolic disorder, primary metabolic disorder, primary-screening tests methylmalonic acidemia methylmalonic aciduria microspherophakia migraine migraine, hemiplegic mitral valve prolapse moyamoya MRI, abnormal MRI, diffusion weighted MRI, venography multiple sclerosis, differential diagnosis of myopia nausea and vomiting neurocutaneous disease neurofibromatosis 1 neurologic examination, focal osteoporosis papilledema paraparesis, spastic pectus excavatum phenylketonuria pleocytosis of cerebrospinal fluid polycythemia, primary prognathism prognosis progressive neurologic disorder protein C deficiency pseudoxanthoma elasticum psychiatric problems in neurologic disorders psychosis pulmonary embolism renal failure renal stones review article risk factors scoliosis scoliosis, neurologic association with seizure short stature sickle cell disease skin, lesions in neurologic disorders subarachnoid hemorrhage superior sagittal sinus thrombosis systemic illness thrombocytopenia thrombophlebitis transient ischemic attack treatment of neurologic disorder tuberous sclerosis urinary incontinence urine test for metabolic disorders vegetarianism venous thrombosis, non-cerebral violent behavior vitamin deficiency Von Hippel Lindau

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