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Case 21 - Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS)

from Part V - Cases

Published online by Cambridge University Press:  08 September 2022

By
Shatha Shafi  and
Blathnaid McCoy
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

EEGneuromonitoringmitochondrial encephalomyopathylactic acidosisand stroke-like episodes (MELAS)nonconvulsive status epilepticus (NCSE)
Type
Chapter
Information
Neuromonitoring in Neonatal and Pediatric Critical Care , pp. 268 - 270
Publisher: Cambridge University Press
Print publication year: 2022

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References

Kaufman, KR, Zuber, N, Rueda-Lara, MA, Tobia, A. MELAS with recurrent complex partial seizures, nonconvulsive status epilepticus, psychosis, and behavioral disturbances: case analysis with literature review. Epilepsy Behav. 2010 Aug;18(4):494–7.Google Scholar
Ribacoba, R, Salas-Puig, J, González, C, Astudillo, A. Characteristics of status epilepticus in MELAS. Analysis of four cases. Neurologia. 2006 Jan-Feb;21(1):1–11.Google Scholar
Demarest, ST, Whitehead, MT, Turnacioglu, S, Pearl, PL, Gropman, AL. Phenotypic analysis of epilepsy in the mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes-associated mitochondrial DNA A3243G mutation. J Child Neurol. 2014 Sep;29(9):1249–56.CrossRefGoogle ScholarPubMed
Karkare, S, Merchant, S, Solomon, G, Engel, M, Kosofsky, B. MELAS with A3243G mutation presenting with occipital status epilepticus. J Child Neurol. 2009 Dec;24(12):1564–7.CrossRefGoogle ScholarPubMed

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