Epileptic encephalopathy, early infantile, 2: A genetic form of epilepsy which is severe and starts during infancy. The condition is considered an atypical form of Rett syndrome due to the development of stereotypical hand movements and repetitive behaviors. This form of the condition is caused by a defect on the CDKL5 gene. More detailed information about the symptoms, causes, and treatments of Epileptic encephalopathy, early infantile, 2 is available below.
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