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"Mitochondrial diseases"

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"Mitochondrial diseases"

Brief Communication

Late-Onset Myopathic form of Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency Linked to Compound Heterozygous Variants in ACADVL
Wonjae Sung, Young-Eun Kim, Seung Hyun Kim
Korean J Neuromuscul Disord 2022;14(2):42-44.   Published online December 31, 2022
DOI: https://doi.org/10.46518/kjnmd.2022.14.2.42
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Case Report
Adult-onset Leigh syndrome due to m.9176T>C mutation with cortical involvement
Hyuk-je Lee, Myungah Lee, Jung Hwan Lee
Ann Clin Neurophysiol 2022;24(2):107-110.   Published online October 31, 2022
DOI: https://doi.org/10.14253/acn.2022.24.2.107
We describe the case of a 22-year-old female complaining of ophthalmoplegia, which deteriorated with seizure. Leigh syndrome (LS) was diagnosed by identifying the m.9176T>C mutation. She improved with vitamin cocktail therapy plus intravenous methylprednisolone, and had an excellent prognosis. This was the first case of an adult patient with LS presenting with the m.9176T>C mutation and reporting cortical symptoms, which in this case comprised cortical vision loss, and cortical, basal ganglia, and brainstem signal changes on magnetic resonance imaging.
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