Rhabdomyolysis: neurological causes
Evidence-based neurology checklist on rhabdomyolysis: neurological causes: Glycogen storage diseases (GSD) GSD type V: McArdle’s disease GSD type VII: Tarui disease GSD type IX GSD type X GSD type XIII Phosphoglycerate kinase 1 deficiency Other metabolic myopathies Muscular dystrophy Mitochondrial…
Glycogen storage diseases (GSD)
- GSD type V: McArdle’s disease
- GSD type VII: Tarui disease
- GSD type IX
- GSD type X
- GSD type XIII
- Phosphoglycerate kinase 1 deficiency
Other metabolic myopathies
Muscular dystrophy
Mitochondrial myopathies
Ryanodine receptor 1 (RyR1) disorders
MLIP myopathy
RHABDO prediction criteria for genetic causes of rhabdomyolysis
Other neurological causes
Acronyms
References
- Huerta-Alardin AL, Varon J, Marik PE. Bench-to-bedside: rhabdomyolysis-an overview for clinicians. Critical Care 2005; 9:158-169.
- Khan FY. Rhabdomyolysis: a review of the literature. Neth J Med 2009; 67:272-283.
- Scalco RS, Gardiner AR, Pitceathly RD, et al. Rhabdomyolysis: a genetic perspective. Orphanet J Rare Dis 2015; 10:51.
- Izumi R, Suzuki N, Nagata M, et al. A case of late onset riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency manifesting as recurrent rhabdomyolysis and acute renal failure. Intern Med 2011; 50:2663-2668.
- Ishii K, Komaki H, Ohkuma A, Nishino I, Nonaka I, Sasaki M. Central nervous system and muscle involvement in an adolescent patient with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency. Brain Dev 2010; 32:669-672.
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