Cargando…
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...
| Autores principales: | , , , , , , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
F1000 Research Limited
2022
|
| Materias: | |
| 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 |