Basal ganglia-based movement abnormalities are the hallmark of the neuropsychiatric presentation of Wilson's disease. Seizures are rarely reported in Wilson's disease, especially as the initial presentation. We report a case of a 17-year-old male who was admitted with recurrent seizures and initially treated as a case of encephalitis and on subsequent follow up diagnosed with Wilson's disease. This case highlights the importance of considering the possibility of Wilson's disease in young patients presenting with unexplained encephalopathy