Epilepsy in KBG syndrome.

Marina AuconiDomenico SerinoMaria Cristina DigilioMaria GnazzoMarta ContiFederico VigevanoLucia Fusco

Published in: Developmental medicine and child neurology (2022)

In our patients, epilepsy appeared to respond well to treatment and, in some cases, to be self-limiting. The molecular characteristics of our patients' genetic abnormalities did not point towards any specific epilepsy hot spot. Epilepsy should be considered in the diagnostic work-up of patients with KBG syndrome.

Keyphrases

end stage renal disease
ejection fraction
newly diagnosed
chronic kidney disease
prognostic factors
case report
genome wide
patient reported outcomes
copy number
patient reported