Case Report: Early Neonatal EEG in Two Infants with Pallister Killian Syndrome (PKS) [version 1; peer review: 2 approved]

Case Report: Early Neonatal EEG in Two Infants with Pallister Killian Syndrome (PKS) [version 1; peer review: 2 approved]

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...

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Bibliographic Details
Main Authors: Niamh McSweeney, Brian McNamara, Geraldine B Boylan, Michael Moore, Carol M Stephens, Andreea M Pavel, Sean R Mathieson
Format: Article
Language:English
Published: F1000 Research Ltd 2022-02-01
Series:HRB Open Research
Subjects:
Neonatal seizures
electroencephalography (EEG)
Pallister-Killian Syndrome
epilepsy
eng
Online Access:https://hrbopenresearch.org/articles/5-14/v1

Internet

https://hrbopenresearch.org/articles/5-14/v1

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