Eyelid myoclonia with absences, intellectual disability and attention deficit hyperactivity disorder: a clinical phenotype of the RORB gene mutation
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DOI: 10.1007/s10072-020-05031-y
Abstract: Eyelid myoclonia with absences is recently included in the category of childhood epileptic syndromes. It is clinically characterized by brief seizures of eyelid myoclonia, sometimes followed by absences, and it is associated to EEG generalized… read more here.
Keywords: myoclonia; absences intellectual; myoclonia absences; gene ... See more keywords
Electroclinical Features and Long-term Seizure Outcome in Patients With Eyelid Myoclonia With Absences
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DOI: 10.1212/wnl.0000000000200165
Abstract: Background and Objectives Eyelid myoclonia (EM) with absences (EMA) is a generalized epilepsy syndrome with a prognosis and clinical characteristics that are still partially undefined. We investigated electroclinical endophenotypes and long-term seizure outcome in a… read more here.
Keywords: long term; seizure; eyelid myoclonia; remission ... See more keywords