Expanding the phenotype of NEDAMSS with a psychiatric perspective: analysis of a new case, and a systematic review of the literature.

Pathogenic variants in the IRF2BPL gene are associated with neurodevelopmental disorders with varying degrees of regression, loss of speech and epilepsy. The phenotype is also known as Neurodevelopmental Disorder with regression, Abnormal Movements, loss of Speech, and Seizures (NEDAMSS). The motor...

Full description

Bibliographic Details

Published in:	European Child & Adolescent Psychiatry Vol. 34; no. 3; pp. 835 - 853
Main Authors:	Kristiansen, Kimmie, Vernal, Ditte Lammers, Hulgaard, Ditte Roth
Format:	case study research systematic review tables/charts Journal Article
Published:	Springer Nature Mar2025
Online Access:	View this record in EBSCOhost