Infantile epileptic-dyskinetic encephalopathy
MONDO:0018226Infantile epileptic-dyskinetic encephalopathy is a monogenic disease with epilepsy characterized by developmental delay and infantile spasms in the first months of life, followed by chorea and generalized dystonia and progressing to quadriplegic dyskinesia, recurrent status dystonicus, intractable focal epilepsy and severe intellectual disability.
17 clinical trials for this condition and its sub-types, 3 tagged with Infantile epileptic-dyskinetic encephalopathy itself.
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