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Epilepsy in Nicolaides–Baraitser Syndrome: Review of Literature and Report of 25 Patients Focusing on Treatment Aspects

Hofmeister, Benedikt ; von Stülpnagel, Celina ; Betzler, Cornelia ; Mari, Francesca ; Renieri, Alessandra ; Baldassarri, Margherita ; Haberlandt, Edda ; Jansen, Katrien ; Schilling, Stefan ; Weber, Peter ; Ahlbory, Katja ; Tang, Shan ; Berweck, Steffen ; Kluger, Gerhard



Zusammenfassung

Nicolaides-Baraitser syndrome (NCBRS), caused by a mutation in the SMARCA2 gene, which goes along with intellectual disability, congenital malformations, especially of face and limbs, and often difficult-to-treat epilepsy, is surveyed focusing on epilepsy and its treatment. Patients were recruited via "Network Therapy of Rare Epilepsies (NETRE)" and an international NCBRS parent support group. ...

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