Molecular and neurological features of MELAS syndrome in paediatric patients: A case series and review of the literature

Molecular and neurological features of MELAS syndrome in paediatric patients: A case series and review of the literature

Abstract Background Mitochondrial encephalomyopathy, lactic acidosis and stroke‐like episodes (MELAS) syndrome is one of the most well‐known mitochondrial diseases, with most cases attributed to m.3243A>G. MELAS syndrome patients typically present in the first two decades of life with a broad, mu...

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Bibliographic Details
Main Authors: Lydia M. Seed, Andrew Dean, Deepa Krishnakumar, Poe Phyu, Rita Horvath, Pooja Devi Harijan
Format: Article
Language:English
Published: Wiley 2022-07-01
Series:Molecular Genetics & Genomic Medicine
Subjects:
encephalopathy
genetics
lactic acidosis
m.3243A>G
MELAS syndrome
mitochondrial disease
Online Access:https://doi.org/10.1002/mgg3.1955

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https://doi.org/10.1002/mgg3.1955

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