O-Store

Malignant Hyperthermia Overview

Malignant Hyperthermia
US$ 75.00 RRP
US$ 67.50 REGISTERED USER PRICE
ADD TO CART

Category: Metabolic - Associated with the enzymes and metabolic processes of cells

Gene: Ryanodine receptor 1 (RYR1) on Chromosome 1

Variant Detected: Base Substitution c.1640T>C p.Val547Ala

Severity: Scale 4 has a high degree of severity. It generally causes a decreased quality of life and may also decrease the life expectancy.

Mode of Inheritance: Autosomal Recessive

Test Overview: Maligant hyperthermia (MH) is an inherited disorder of skeletal muscle characterized by hypercarbia, rhabdomyolysis, generalized skeletal muscle contracture, cardiac dysrhythmia, and renal failure, that develops on exposure to succinylcholine or volatile anesthetic agents. Specific interventions, including use of the calcium release channel antagonist dantrolene, are efficacious in reversing signs of the canine syndrome.

Research Citation(s): Roberts MC, et al. Autosomal dominant canine malignant hyperthermia is caused by a mutation in the gene encoding the skeletal muscle calcium release channel (RYR1). (2001) Anesthesiology 95;716-725.

Associated Breed(s): Labradoodle ,  Greyhound ,  Labrador Retriever,  German Shorthaired Pointer,  Australian Labradoodle ,  Australian Cobberdog,  Mixed Breed,