A case report of malignant hyperthermia in a patient with myotonic dystrophy type I: A CARE-compliant article

RATIONALE: Several hereditary myopathies that can predispose to malignant hyperthermia (MH) are reported. However, the risk of MH in myotonic dystrophy type I (DM1) has been suggested equal to general population, although the evidence is limited to only a few case reports. PATIENT CONCERNS: We encou...

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Detalles Bibliográficos
Autores principales: Yoo, Seon Woo, Baek, Seon Ju, Kim, Dong-Chan, Doo, A Ram
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
3300
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8202553/
https://www.ncbi.nlm.nih.gov/pubmed/34114984
http://dx.doi.org/10.1097/MD.0000000000025859

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8202553/
https://www.ncbi.nlm.nih.gov/pubmed/34114984
http://dx.doi.org/10.1097/MD.0000000000025859

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