Case Report: Early Neonatal EEG in Two Infants with Pallister Killian Syndrome (PKS)

Pallister Killian Syndrome (PKS) is a rare genetic disorder caused by a mosaic tetrasomy of the short arm of chromosome 12. The syndrome is characterised by typical craniofacial dysmorphism, congenital anomalies and intellectual disability. Epilepsy is a known complication, with onset usually occurr...

Descripción completa

Detalles Bibliográficos
Autores principales: Stephens, Carol M, Pavel, Andreea M, Mathieson, Sean R, McSweeney, Niamh, McNamara, Brian, Moore, Michael, Boylan, Geraldine B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000 Research Limited 2022
Materias:
Clinical Practice Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9530620/
https://www.ncbi.nlm.nih.gov/pubmed/36249954
http://dx.doi.org/10.12688/hrbopenres.13493.1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9530620/
https://www.ncbi.nlm.nih.gov/pubmed/36249954
http://dx.doi.org/10.12688/hrbopenres.13493.1

Ejemplares similares