Publications by authors named "Angeline Charmet"
Article Synopsis
- * The report details a case of a 5-year-old boy with a deletion mutation in the KCNQ2 gene, diagnosed with seizures, autism, and intellectual deficiency linked to KCNQ2-encephalopathy.
- * The findings emphasize the need for genetic counseling and psychiatric evaluation to better manage the complex social and behavioral aspects of these conditions.