Acute onset of diabetes and rapid cognitive decline in a patient with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes syndrome

SUMMARY: Mitochondrial diseases are a group of rare diseases presenting with heterogeneous clinical, biochemical, and genetic disorders caused by mutations in the mitochondrial or nuclear genome. Multiple organs can be affected, particularly those with high energy demand. Diabetes is a common endocr...

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Detalles Bibliográficos
Autores principales: Tran, Nam Quang, Phan, Chien Cong, Vuong, Tran Bao, Tran, Thang Viet, Ma, Phat Tung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2023
Materias:
Unique/Unexpected Symptoms or Presentations of a Disease
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10241238/
https://www.ncbi.nlm.nih.gov/pubmed/37073829
http://dx.doi.org/10.1530/EDM-22-0416

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10241238/
https://www.ncbi.nlm.nih.gov/pubmed/37073829
http://dx.doi.org/10.1530/EDM-22-0416

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