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Article

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

Medicine - 11 Jun 2021

Yoo Seon Woo, Baek Seon Ju, Kim Dong-Chan, Doo A Ram

Abstract excerpt

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 encountered a rare case of MH during anesthesia induction with sevoflurane in a male adolescent with previously...

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 34114984
DOI: 10.1097/MD.0000000000025859
PMCID: PMC8202553

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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