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Malignant hyperthermia mutations and correlation with the severity of the anesthetic complication and the level of the in vitro contracture tests

✍ Scribed by René Krivosic-Horber,Anne-Frédérique Dalmas,Etienne Brasdefer…

Book ID
126370683
Publisher
BioMed Central
Year
2014
Tongue
English
Weight
206 KB
Volume
14
Category
Article
ISSN
1471-2253

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Malignant hyperthermia (MH) is an autosomal dominant disorder characterized by abnormal calcium homeostasis in skeletal muscle in response to triggering agents. Today, genetic investigations on ryanodine receptor type 1 (RYR1) gene and alpha1 subunit of the dihydropyridine receptor (DHPR) (CACNA1S)