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purpura/epileptische aanval

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Contrast-induced seizure associated with thrombotic thrombocytopenic purpura. Case report.

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A patient with thrombotic thrombocytopenic purpura had a seizure as the result of a contrast media injection given during computed tomographic examination. To our knowledge, ours is the first such case reported.

A rare presentation of seizures in a not-so-rare disease: Henoch-Schönlein purpura presenting with repeated seizures.

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Henoch-Schönlein purpura represents the most common form of systemic vasculitis in children. Although a very common cause of vasculitis, seizures are a very rare complication of this disorder. We report a 5-year-old boy who presents with no other clinical symptoms of the disorder other than a
OBJECTIVE To analyze the clinical features and SLC25A13 gene mutations of a child with citrin deficiency complicated with purpura, convulsive seizures and methioninemia. METHODS The patient was subjected to physical examination and routine laboratory tests. Blood amino acids and acylcarnitines, and
We present a case of hereditary thrombotic thrombocytopenic purpura (hTTP) caused by a previously undescribed mutation in a 36-year-old woman who presented with seizures in the context of a possible infection. Her hematologic manifestations were mild, despite undetectable ADAMTS13 (A Distintegrin

Seizures, renal failure and acute respiratory failure: not your typical case of Henoch-Schonlein purpura.

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A 30-year-old Caucasian woman with no prior medical history presented with pedal oedema, arthralgias and abdominal pain with diarrhoea, following a respiratory infection. She had mild abdominal tenderness along with a purpuric rash on the extremities and was anaemic. Following initial workup for

Seizures complicating adult Henoch-Schönlein purpura.

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[Seizure-related purpura].

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Seizure-induced purpura: a rare but useful clue.

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Post-seizure purpura of the head and neck.

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Seizure in patients with thrombotic thrombocytopenic purpura.

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Thoracocervicofacial purpura as the single manifestation of epileptic seizure.

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[Febrile convulsion revealing thrombotic thrombocytopenic purpura].

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A 46-year-old woman with systemic lupus erythematosus was hospitalized for purpura, hematochezia and hematuria. One week after admission, she developed grand mal seizures and coma and was diagnosed with thrombotic thrombocytopenic purpura (TTP) when fragmented red cells were found on the peripheral

Treatment of status epilepticus with plasmapheresis in a patient with thrombotic thrombocytopenic purpura.

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Thrombotic thrombocytopenic purpura (TTP) is a syndrome with numerous neurological manifestations including altered mental status and seizures. However, status epilepticus (SE) has rarely been reported in this condition. Signs may be transient or fluctuate; however, permanent deficits do occur. Its
Neurological complications are rare during the course of Henoch-Schönlein purpura (HSP). We report a 7-year-old girl with HSP who presented with seizures, loss of vision and disturbance of consciousness. Magnetic resonance imaging (MRI) showed high signal intensity in the gray and white matter over
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