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hepatic encephalopathy
progresses rapidly, presence of waxing and waning cerebral dysfunction in the setting of liver failure.
impaired attention and concentration, altered sleep patterns, abnormal visuospatial perception, and subtle personality changes. Increased muscle tone, hyperreflexia, and extensor plantar responses
due to accumulation of neurotoxic substances leading to increased brain glutamine concentrations, depressed glutamatergic neurotransmission, and increased expression of the peripheral-type benzodiazipine receptors
path: alzheimer type II astrocyte that are metabolically hyperactive
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neurologic manifestations of systemic disease...
polyarteritis nodosa
mononeuropathy multiplex, seizures, stroke
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neurologic manifestations of systemic disease...
churg-strauss
mononeuropathy multiplex, encephalopathy, stroke, chorea
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neurologic manifestations of systemic disease...
giant cell arteritis
headache, blindness, polyneuropathy, stroke
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neurologic manifestations of systemic disease...
wegner granulomatosis
mononeuropathy multiplex, cranial neuropathy, basal meningitis
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neurologic manifestations of systemic disease...
rheumatoid arthritis
myelopathy
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neurologic manifestations of systemic disease...
sjogren syndrome
sensory polyneuropathy
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neurologic manifestations of systemic disease..
behcet disease
aseptic meningoencephalitis
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neurologic manifestations of systemic disease...
cryoglobulinemia
TIA, stroke, peripheral neuropathy
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neurologic manifestations of systemic disease...
DIC
encephalopathy
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neurologic manifestations of systemic disease...
thrombotic thrombocytopenic purpura
encephalopathy, seizures, stroke
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neurologic manifestations of systemic disease...
whipple disease
dementia, seizures, myoclonus, atazia, supranuclear ophthalmoplegia, oculomasticatory myorhythmia
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neurosarcoidosis
pulmonary disease most common in sarcoidosis but can affect any part of the nervous system
chronic neuropathy due to chronic basal meningitis is most common presentation, with facial and optic nerves most frequently affected. facial neuropathy may also be due to parotid inflammation
path: non-caseating granulomata. CSF ACE may be elevated, tx with steroids
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disorders characterized by noth diabetes and neurologic symptoms
- mitochondrial diseases
- myotonic dystrophy
- Friedrich ataxia
- stiff-man syndrome
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diabetes neuro
predilection for involvement of small myelinated and unmyelinated fibers, with resulting loss of temperature and pinprick sensation. associated autonomic neuropathy (gustatory sweating, orthostatic hypotension, diarrhea, and impotence)
thoracic radiculopathy - truncal sensory loss, focal weakness of muscles of anterior abdominal wall, nonradicular pain
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diabetic amyotrophy
proximal diabetic neuropathy
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nonketotic hyperglycemia neuro symptoms
lethargy and drowsiness with focal or generalized seizures, sometimes dystonia of chorea
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hypoglycemia neuro symptoms
headache, blurred vision, dysarthria, confusion, seizures, and coma. repeated episodes may produce injury to anterior horn cells of spinal cord resulting in syndrome similar to ALS
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deficiency of thiamine, niacin
confusion and encephalopathy
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deficiency of B12, folate, niacin
dementia
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deficiency of pyridoxine, niacin
seizures
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deficiency of vit E, niacin
ataxia
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deficiency of B12, E, niacin
myelopathy
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deficiency of thiamine, pyridoxine, B12, E, niacin
peripheral neuropathy
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Wernike's encephalopathy
opthalmoplegia, truncal ataxia, confusion developing over days or weeks
may be precipitated by the administration of IV glucose
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Subacute combined degeneration of spinal cord
B12 deficiency
degeneration of posterior and lateral white matter tracts of the spinal cord. dorsal columns and lateral cotricospinal tracts. presentation insidious onset of paresthesias in hands and feet with weakness and spasticity in legs. large-fiber peripheral neuropathy, macrocytic anemia.
normal serum B12 levels do NOT preclude diagnosis, need to measure levels of serum homocysteine and methylmalonic acid (elevated when B12 deficient)
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antiphospholipid syndrome
venous or arterial thrombosis, recurrent fetal loss, and thrombocytopenia are associated with elevated titers of antibodies against phospholipids.
young pts with stroke, suspect. diagnosis requires demonstration of high-titer IgG antiphopholipid antibodies on 2 occasions at least 6 weeks apart
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Neurologic manifestations of hypothyroidism
- mental state: poor concentration and memory, dementia, psychosis, coma
- seizures
- headaches: pseudotumor cerebri
- cranial nerves: papilledema, ptosis, tonic pupil, trigeminal neuralgia, facial palsy, tinnitus, and hearing loss
- cerebellar ataxia: truncal and gait ataxia more than limb ataxia, dysarthria, nystagmus
- muscles: cramps, pain and stiffness, proximal more than distal, CK may be increased
- worsening of myasthenia gravis
- nerves: entrapment neuropathy, axonal polyneuropathy (improves with thyroxine replacement), delayed relaxation of DTRs
- sleep apnea: central and obstructive
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neuro symptoms of hyperthyroidism
periodic paralysis and proximal myopathy, seizures, chorea, and dysarthria, association with myasthenia gravis
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central pontine myelinolysis
demyelinating disorder often in alcoholic pts, may be precipitated by too rapid correction of hyponatremia
presents with acute confusional state, spastic quadriparesis, locked-in syndrome, dysarthria, and dysphagis
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