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852 Possible Causes for Hypovolemia, Seizure

  • Subarachnoid Hemorrhage

    Corticosteroids, specifically hydrocortisone and fludrocortisone, decreased natriuretic diuresis and incidence of hypovolemia.[] None of the patients with epilepsy after discharge had electrographic seizures while hospitalized.[] Its use is associated with prevention of hyponatremia and hypovolemia through their mineralocorticoid effect.[]

  • Cerebral Salt-Wasting Syndrome

    We started normal saline for hypovolemia, each 1 L prior and after amphotericin therapy. However, hypovolemia did not improve significantly despite IV fluid.[] A 2-year-old male patient presented to our hospital due to a seizure attack. He had been neglected and refused to take food for a long time (body weight 3rd percentile).[] She presented 16 days postoperatively, and following two grand mal seizures was found to be profoundly hyponatraemic (sodium 101 nmol/l).[]

  • Hepatic Encephalopathy

    Overdosage can result in ileus, severe diarrhea, electrolyte disturbances, and hypovolemia.[] The 59-year-old patient had esophageal varices bleeding due to primary biliary cirrhosis (ammonium blood level: 140 mmoL/L) and presented with sensory Jacksonian seizures,[] 30 and 45 percent of people with cirrhosis will develop some signs of hepatic encephalopathy, whether it be mild forms of forgetfulness or more severe bouts of amnesia or seizures[]

  • Angioedema

    To help address this question, the Observational Health Data Sciences and Informatics research network conducted a retrospective observational new-user cohort study of seizure[]

  • Hyponatremia

    CASE REPORT: Here, we present the case of an HIV patient presenting with hyponatremia and a physical examination suggestive of hypovolemia.[] Post-transplant seizures are uncommon in young kidney transplant recipients but can be harbingers of devastating outcomes such as cerebral edema and death.[] Hypovolemia can also be due to diabetes mellitus-associated complications, such as diarrhea and vomiting.[]

  • Amanita Phalloides Poisoning

    The fluid loss may progress to hypovolemia, electrolyte disturbances and circulatory shock. The levels of liver enzymes and bilirubin are usually normal at this stage.[] Intoxication symptoms usually appear after a latent period and may include gastrointestinal disorders followed by jaundice, seizures, and coma, culminating in death.[] […] and renal failure, encephalopathy Cyclopeptides Amatoxin Phallotoxin Virotoxin 6 to 12 hours 24 to 36 hours Days to weeks Gastroenteritis, dizziness, headache, intractable seizures[]

  • Purging-Type Bulimia Nervosa

    In addition to anorexia, a number of disorders may mimic bulimia, including: borderline personality disorder brain tumors depression epileptic seizures Klein-Levin syndrome[] […] parallel those used to treat depression, but higher doses of fluoxetine ( 80 mg/day) may be needed to treat bulimia nervosa. 51 Bupropion (Wellbutrin) has been associated with seizures[] Hypophosphatemia can manifest as weakness, confusion, seizures and rhabdomyolysis; additional clinical features of refeeding syndrome are associated with different electrolyte[]

  • Hereditary Angioedema

    Additional rare physical findings that have been reported are pleuritic symptoms with pleural effusions, seizures and hemiparesis secondary to cerebral edema, and bladder[] Others 9, 16, 17 have reported seizures and hemiparesis.[]

  • Diffuse Cerebral Sclerosis of Schilder

    […] damaged or die, such as Parkinson's disease and Alzheimer's disease Diseases of the blood vessels that supply the brain, such as stroke Injuries to the spinal cord and brain Seizure[] Clinical findings Onset at age 5 and 10 with reversal of neurologic milestones, seizures, ataxia, Addison's disease, degeneration of visual and auditory function.[] Variable neurological abnormalities progressively develop and include personality changes, poor attention, dementia, aphasia, headache, vomiting, tremor, seizures, balance[]

  • Hereditary Angioedema Type 1

    Hereditary angioedema type 1 is an autosomal dominant disease characterized by C1 esterase inhibitor deficiency and the onset of edema, abdominal pain and erythema marginatum. Clinical features of HAE are largely indistinguishable across all types, but type 1 is characterized by a prodromal period in which a[…][]

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