Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression

MONDO:0018314

A rare monogenic disease with infantile-onset pharmacoresistant focal seizures of mesial temporal lobe onset manifesting with unresponsiveness, hypertonia and automatisms and cognitive regression soon after seizure onset leading to severe intellectual disability with behavioral abnormalities.

7 clinical trials for this condition and its sub-types, 0 tagged with Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression itself.

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