Other Names for this Disease
- Anesthesia related hyperthermia
- Malignant hyperpyrexia
- Fulminating hyperpyrexia
- Pharmacogenic myopathy
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autosomal dominant manner. People with certain inherited muscle diseases (e.g., central core disease and multiminicore disease) also have MH susceptibility.Malignant hyperthermia (MH) is a severe reaction to certain gases used during anesthesia and/or a muscle relaxant used to temporarily paralyze a person during surgery. Signs and symptoms of MH include marked hyperthermia, a rapid heart rate, rapid breathing, acidosis, muscle rigidity, and breakdown of muscle tissue (rhabdomyolysis). Without prompt treatment, MH can be life-threatening. People who are at increased risk for this reaction are said to have MH susceptibility. Susceptibility to MH may be caused by mutations in any of several genes and is inherited in an
Last updated: 6/30/2014
- Malignant Hyperthermia. Genetics Home Reference. 2007; http://ghr.nlm.nih.gov/condition/malignant-hyperthermia. Accessed 4/4/2011.
- Mark Davis, Danielle James, Neil Pollock, Henry Rosenberg, Kathryn Stowell. Malignant hyperthermia. Orphanet. April, 2007; http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=423. Accessed 6/30/2014.
- Genetics Home Reference (GHR) contains information on Malignant hyperthermia. This website is maintained by the National Library of Medicine.
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- Online Mendelian Inheritance in Man (OMIM) is a catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine.
- Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge.
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