Developmental progression of intellectual disability, autism, and epilepsy in a child with an IQSEC2 gene mutation
Rachelle Zipper1, Sherri D Baine2, Jacob Genizi1,3
1Technion Faculty of Medicine Technion Israel Institute of Technology Haifa Israel.
Clinical Case Reports
|October 14, 2017
Abstract:
The neurodevelopmental progression of a school-aged child with a spontaneous IQSEC2 mutation has demonstrated apparent regression of milestones and language. Seizures associated with the disorder have been refractory to medical treatment. Late treatment of autism in this child has led to improved social skills.
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