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Case 11 - Hemimegalencephaly

from Part V - Cases

Published online by Cambridge University Press:  08 September 2022

By
Jonathan D. Santoro  and
Courtney J. Wusthoff
Edited by
Cecil D. Hahn  and
Courtney J. Wusthoff
Cecil D. Hahn
Affiliation:
The Hospital for Sick Children, University of Toronto
Courtney J. Wusthoff
Affiliation:
Lucile Packard Children’s Hospital, Stanford University
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Summary

n/a

Keywords

neonateEEGneuromonitoringseizurehemimegalencephaly
Type
Chapter
Information
Neuromonitoring in Neonatal and Pediatric Critical Care , pp. 237 - 239
Publisher: Cambridge University Press
Print publication year: 2022

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References

Flores-Sarnat, L. Hemimegalencephaly: part 1. Genetic, clinical, and imaging aspects. J Child Neurol. 2002 May;17(5):373–84. PMID: 12150586.CrossRefGoogle ScholarPubMed
D’Agostino, MD, Bastos, A, Piras, C, et al. Posterior quadrantic dysplasia or hemi-hemimegalencephaly: a characteristic brain malformation. Neurology. 2004 Jun 22;62(12):2214–20. PMID: 15210885.Google Scholar
Di Rocco, C, Battaglia, D, Pietrini, D, Piastra, M, Massimi, L. Hemimegalencephaly: clinical implications and surgical treatment. Childs Nerv Syst. 2006 Aug;22(8):852–66. PMID: 16821075.Google Scholar
Honda, R, Kaido, T, Sugai, K, et al. Long-term developmental outcome after early hemispherotomy for hemimegalencephaly in infants with epileptic encephalopathy. Epilepsy Behav. 2013 Oct;29(1):30–5. PMID: 23933627.CrossRefGoogle ScholarPubMed

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