subacute sclerosing panencephalitis/seizures

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Subacute sclerosing panencephalitis with generalized seizure as a first symptom: a case report.

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Subacute sclerosing panencephalitis (SSPE) can show variations in its clinical course. Typical initial symptoms consist of intellectual decline, deterioration in school performance, and myoclonic jerks. Atypical forms of presentation such as generalized seizures and acute or subacute coma can be

A case of subacute sclerosing panencephalitis preceded by epileptic seizures: evolutional EEG changes.

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We reported a patient with subacute sclerosing panencephalitis (SSPE) in whom EEG had been serially performed before the onset. She was referred to our hospital due to epileptic seizures at 2 years of age. Focal spikes were seen on EEG at the time of her first seizure (2 years 4 months). At the time

Seizures in a boy with subacute sclerosing panencephalitis during high-dose intrathecal interferon-alpha therapy.

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A 27-month-old boy was admitted with speech abnormality, inability to walk, and involuntary movements. He was diagnosed with subacute sclerosing panencephalitis based on clinical and laboratory findings. Inosiplex (100 mg/kg/day orally) plus intrathecal interferon-alpha (3 million units/dose twice

Tonic seizures in subacute sclerosing panencephalitis: a video-illustration of two cases.

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Subacute sclerosing panencephalitis is a progressive disorder which also presents with various types of seizures, mainly myoclonic jerks, atonic attacks and tonic-clonic seizures. We report two cases, documented by video-EEG that during the course of the disease also presented with tonic seizures.

[Epileptic seizures and epilepsy in subacute sclerosing panencephalitis (report of 30 cases].

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Subacute Sclerosing Panencephalitis (SSPE) is becoming less frequent in Morocco since the generalization of measles vaccination in 1982. The aim of this study was first to analyze the semiological and elecrophysiological profiles of epilepsy in SSPE in both 'disease-revealing' seizures and sequellar

Adult-onset subacute sclerosing panencephalitis presenting with tonic motor seizures.

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Purpose/aim of the study: Subacute sclerosing panencephalitis (SSPE) is a degenerative disease of the brain caused by a persistent measles virus infection occurring mostly in childhood or early adolescence. The spectrum of epileptic phenomena associated with SSPE is wide, varying from partial

Subacute sclerosing panencephalitis presenting as simple partial seizures.

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Subacute sclerosing panencephalitis is reported in a 16-year-old girl with a 2 1/2-year history of right-sided simple partial sensory and motor seizures. The seizures were verified with video-electroencephalographic monitoring, showing left frontal epileptic activity. After an initial response to

Subacute sclerosing panencephalitis in a child with recurrent febrile seizures.

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Subacute sclerosing panencephalitis (SSPE) is a devastating disease of the central nervous system (CNS) caused by persistent mutant measles virus infection. The diagnosis of SSPE is based on characteristic clinical and EEG findings and demonstration of elevated antibody titres against measles in

Case of subacute sclerosing panencephalitis with atypical absences and myoclonic-atonic seizures as a first symptom.

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The 2-year history of a 10-year-old boy with subacute sclerosing panencephalitis is presented. After 6 months of epilepsy manifested by atypical absences and myoclonic-atonic seizures with an electroencephalographic (EEG) correlation of generalized spike-and polyspike-wave discharges, the child

Generalized sharp and slow wave and electrodecremental seizure pattern in subacute sclerosing panencephalitis.

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Although subacute sclerosing panencephalitis (SSPE) often presents with a characteristic EEG pattern, a 13-year-old boy with a confirmed diagnosis of SSPE had several EEG features that are unusual for this condition, namely, generalized sharp and slow wave (slow spike and wave) discharges during the

[Complex partial epileptic seizures as the initial symptom of subacute sclerosing panencephalitis].

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A 18 year-old boy, without a previous history, presented with psychomotor seizures and, 4 months after, mental deterioration. EEG showed focal epileptic abnormalities characterized by high amplitude spike waves in the left temporal region. Periodic complexes appeared after administration of

Cluster of partial motor seizures heralding the onset of hemimyoclonic subacute sclerosing panencephalitis.

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[Clinico-electroencephalographic correlates in subacute sclerosing panencephalitis].

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The authors studied 30 cases of subacute sclerosing panencephalitis in various stages of the disease. The group comprised 28 children with a mean age of 7.8 years and 2 adults ages 22.5 years on the average, who were in remission. Apart from characteristic EEG findings with rhythmic seizure activity

Early onset and rapidly progressive subacute sclerosing panencephalitis after congenital measles infection.

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We report an 18-month-old girl with rapidly progressive subacute sclerosing panencephalitis, whose non immunised mother had measles at the time of delivery. The patient presented with repetitive episodes of myoclonic jerks of the head and arms, followed by a drop of head and trunk with frequent

[Subacute Sclerosing Panencephalitis Presenting Initially as Schizophrenic Psychosis in a 19-Year Old Man]

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We report the rare case of a 19-year old man, first diagnosed with schizophrenia but finally shown to have subacute sclerosing panencephalitis (SSPE). Initial symptoms were hallucinations and negative symptoms until the onset of a seizure. Changes in the CSF, MRI, EEG and increasing neurological

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