EEG-mediated diagnosis of an unusual presentation of SSPE.

Clin Neurophysiol

Epilepsy and EEG Unit, University Hospital, 1211 14, Geneva, Switzerland.

Published: April 2003

AI Article Synopsis

  • The study focuses on the use of EEG (electroencephalogram) in diagnosing SSPE (subacute sclerosing panencephalitis) in an 18-month-old girl.
  • The EEG showed specific abnormal patterns that matched with muscle atonia episodes observed in the patient.
  • The findings, along with biological tests and MRI scans, confirmed SSPE, showcasing EEG's significance in such rare cases.

Article Abstract

Objective: To highlight the role of EEG in the diagnosis of SSPE.

Methods: EEG was performed in an 18 month old girl who had a 1 week history of repeated episodes of sudden flexion of the head and trunk and frequent falls.

Results: EEG abnormalities consisted of stereotyped, generalized and synchronous high amplitude periodic complexes. These abnormalities correlated with brief episodes of axial and upper limb atonia on electromyogram examination. They persisted during sleep although abnormal movements disappeared. Biological results and cerebral MRI confirmed the diagnosis of subacute sclerosing panencephalitis.

Conclusions: This case is exceptional because of the age of the patient, the clinical presentation and the mode of contamination and it highlights the role of EEG in this diagnosis.

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Source
http://dx.doi.org/10.1016/s1388-2457(02)00306-1DOI Listing

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