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