RT Book, Section A1 Valente, Kette D. A2 Duchowny, Michael A2 Cross, J. Helen A2 Arzimanoglou, Alexis SR Print(0) ID 1138411279 T1 Epilepsy Associated with Chromosomal Disorders T2 Pediatric Epilepsy YR 2017 FD 2017 PB McGraw-Hill Education PP New York, NY SN 9780071496216 LK accesspediatrics.mhmedical.com/content.aspx?aid=1138411279 RD 2024/10/04 AB Many chromosomal anomalies are associated with childhood-onset epilepsy with distinctive features. Accurate electroclinical delineation helps identify chromosomal anomalies in infants classified with cryptogenic epilepsy. Chromosomal disorders carry distinct risks of recurrence making accurate classification important for proper genetic counseling.