01392caa a2200205   4500008004100000022001400041100002100055245005000076260000900126300001400135490002300149520075700172653006400929700002000993700002801013700002201041700003301063773004701096856004301143210629s9999    xx            000 0 und d  a2320-5407  aSowmya. N. Ghosh 0aLANDAU- KLEFFNER SYNDROME: A RARE CASE REPORT  c2017  a1030-1032  vVolume 5  Issue 10  aA 9 year old male presented with history of loss of speech and seizure disorder for two years duration. The boy was developmentally normal before the onset of seizures. Examination of higher mental function revealed excessive hyperactivity, self destructive behaviour and decreased attention span. Audiological evaluation showed bilaterally normal hearing thresholds and he started communicating with signs. EEG showed repetitive spike and epileptiform activity from bilateral parieto-occipital regions. Clinical features and EEG led to a diagnosis of Landau Kleffner Syndrome (LKS). Child was started on steroid, anti-epileptic drug, speech and behavioural therapy immediately and improvement in the symptoms and reduced seizure activity was observed.  aectroencephalography, Steroids, Acquired aphasia, Seizures.  aAbhilash, S      aRajeshwari Govindaswamy  aSundara Raju. H    aTumkur Kumaraswamy Prakash    aInternational Journal of Advanced Research  uhttp://dx.doi.org/10.21474/IJAR01/5621