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American Journal of Autism
We report two cases diagnosed with Tuberous Sclerosis Complex (TSC) that showed relatively late onset developmental regression with loss of skills following onset of epileptic spasms at around two years of age. Both the cases were reported to be developing normally before the regression. The regression in both children was characterised by a sudden and dramatic loss of intellectual abilities, social, communication and play skills and the emergence of autistic symptoms. The loss of skills in onedoi:10.7726/aja.2013.1001 fatcat:y5q5ociiuncezdeydpzs6oleai