Case report: Transient lactate elevation by intravenous insulin infusion therapy for diabetic ketoacidosis in a patient with mitochondrial DNA 3243 A > G mutation: A glycolysis rebooting syndrome?

Mitochondrial disease, most cases of which are caused by mitochondrial DNA (mtDNA) mutation, is present with multiple phenotypes including diabetes mellitus, sensorineural hearing loss, cardiomyopathy, muscle weakness, renal dysfunction, and encephalopathy, depending on the degree of heteroplasmy. W...

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Detalles Bibliográficos
Autores principales: Ohwada, Wataru, Kouzu, Hidemichi, Sato, Tatsuya, Sazawa, Kahomi, Matsui, Azumi, Nagano, Nobutaka, Koyama, Masayuki, Ogasawara, Noriko, Takada, Akifumi, Yano, Toshiyuki, Furuhashi, Masato
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Cardiovascular Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10149661/
https://www.ncbi.nlm.nih.gov/pubmed/37139126
http://dx.doi.org/10.3389/fcvm.2023.1144925

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