Genetic testing with a panel of genes associated with rhabdomyolysis [10] confirmed presence of the “A-” G6PD variant (c.[202G>A; 376A>G] p.[Val68Met; Asn126Asp]) and a heterozygous variant of unknown significance in the dysferlin gene (DYSF c.4510G>A p.Val1504Ile). The gene discussed is DYSF; the disease is rhabdomyolysis.