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Figure 1 | Orphanet Journal of Rare Diseases

Figure 1

From: Rhabdomyolysis: a genetic perspective

Figure 1

Examples of conditions associated with RM. In individual cases both genetic and environmental factors may combine to trigger a RM event; anaesthesia-induced RM is the best characterized example. VLCAD: very long-chain acyl-CoA dehydrogenase, CPTII: carnitine palmitoyl-transferase-II, MAD: multiple acyl-CoA dehydrogenase, GSD: glycogen storage disease, tRNA: Transfer Ribonucleic Acid, DGUOK: deoxyguanosine kinase gene, RYR1: Ryanodine Receptor 1 gene, SIL1: SIL1, S. Cerevisiae, homolog of, TSEN54: tRNA splicing endonuclease 54 gene, S. cerevisiae, homolog of, DMD: Duchenne Muscular Dystrophy, BMD: Becker Muscular Dystrophy, ANO5:Anoctamin 5 gene, LGMD: Limb-girdle Muscular Dystrophy, DYSF: Dysferlin gene, FKRP: fukutin-related protein gene [1,2,4,8,62,110-113].

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