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Страница 1 од 266 резултати
[Ross syndrome presenting with asymptomatic tonic pupils].
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A 66-year-old woman presented with asymptomatic tonic pupils and areflexia when she was admitted to our hospital due to vertigo. She had also noticed heat intolerance and decreased sweating on her right side since she was approximately 10 years old. Both sides of each eye contracted in the
A case of clozapine-induced tonic-clonic seizures managed with valproate: implications for clinical care.
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We describe a case of clozapine-induced seizures in a patient with treatment-resistant schizophrenia. She had previously been treated unsuccessfully with a number of atypical antipsychotic medications, before she was eventually started on clozapine. She experienced two separate episodes of observed
Suicide soon after generalized tonic-clonic seizure. A possible peri-ictal phenomenon?
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We report the case of 36-year-old woman who had suffered from focal-unilateral right febrile grand mal since she was 9 months old as a result of neonatal asphyxia. Over the years, a modification of the clinical picture occurred and eventually the patient suffered from paranoid delusions that
Bilateral tonic pupil secondary to migraine in a child.
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Bilateral idiopathic tonic pupil is characterized by enlarged pupils, poor response to light and accommodation, strong and tonic response to near stimuli, vermiform movements of the iris on slit-lamp examination, and cholinergic supersensitivity. The authors present a case of a 10-year-old girl who
[Subacute sensory neuropathy manifestated by tonic pupils associated with small cell carcinoma of the lung].
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Only a few cases of carcinomatous neuropathy with tonic pupils have been reported. In the present paper we described a 53-year-old woman with subacute sensory neuropathy who had presented with bilateral tonic pupils. She noticed numbness over the medial aspect of the left thigh in March, 1988, and
Successful treatment of paroxysmal tonic spasms with topiramate in a patient with neuromyelitis optica.
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A 49-year-old woman with neuromyelitis optica (NMO) developed severe quadriplegia and frequent paroxysmal tonic spasms (PTS). Carbamazepine, although initially effective against PTS, caused drug eruption and she was unable to continue. PTS re-emerged after discontinuation of carbamazepine and
Tonic-clonic seizure after unrecognized unintentional dural puncture
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Patients that suffer an unintentional experiencing inadvertent dural puncture have a high risk of developing a post-dural puncture headache. Other neurologic complications have been reported, but seizure is rarely seen. We present a case of a 21-year-old primigravida who experienced an unintentional
[A case report of a patient with sequelae of SMON and painful tonic seizure].
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We reported a case with sequelae of SMON and painful tonic seizure (PTS). The patient was a 50-year-old woman. Onset of SMON was when she was 28 years old. She has been suffering from decreased sensation and dysesthesia below C8 cord level to a severe degree, gait disturbance to a moderate degree
Recurrent tonic-clonic seizures and coma due to ingestion of Type I pyrethroids in a 19-month-old patient.
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BACKGROUND
Pyrethroids are synthetic pyrethrin analogues that induce sodium-channel depolarization and hyperexcitation. Severe pyrethroid poisoning is manifested by a "Tremor Syndrome" (Type I cyano-agents) or a "Choreoathetosis/Salivation Syndrome" (Type II non cyano-agents). Very few reports of
[A 85-year-old woman with one year history of convulsion, dementia, and consciousness disturbance].
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We report a 85-year-old woman who died after one year history of convulsion, dementia, and consciousness disturbance. She was apparently well until January 6, 1995 when she was 85 year old; on that evening, she suddenly stated that some one was in her room and she became confused. A local MD gave
Dextromethorphan abuse masquerading as a recurrent seizure disorder.
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Dextromethorphan (DXM) has unique toxicity that may be difficult to diagnose. We present a case of a young woman who presented to our emergency department (ED) initially diagnosed with recurrent seizures. Paramedics brought a 19-year-old woman to the ED. Witnesses noted "shaking," which the patient
[A case of neonatal convulsions caused by transitory normocalcemic primary hypomagnesemia. Clinical considerations].
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The Authors present a case of a primitive normocalcemic hypomagnesimy in a four days newborn. She was hospitalized for convulsive disorders at the Maternity Hospital Foggia - Neonatal Pathology Section. Although her birth had been normal and she was in good condition, the four days infant had clonic
[Lúpus erythematosus].
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Systemic Lúpus Erythematosus (SLE) is an auto-imune disorder, with multiple organ involvement, characterized by vascular and connective tissue inflammation, as well as antinuclear antibodies (ANA). We report a case of a black teenager with a past of arthritis of knees, fever and astenia during the
"BABY, BABY I'VE GOT HEADACHE".
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A 26-year-old woman with no prior medical history presented post-partum with altered mental status. She had no complications during pregnancy and had a spontaneous vaginal delivery at term one week prior. On post-partum day five, she began complaining of headaches, initially responsive to ibuprofen
Streptococcal pharyngitis: an uncommon cause of subdural empyema.
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A 7-year-old girl with an unremarkable medical history presented to a local paediatric emergency department with a 7-day history of fever, sore throat and vomiting, and a 1-day history of rash. She was admitted to the hospital, with presumed Kawasaki disease. A few hours after admission, the patient
Најкомплетната база на податоци за лековити билки поддржана од науката
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