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MYOGLOBINURIA - RHABDOMYOLYSIS

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Overview

From WUSTL Neuromuscular

Myoglobinuria Malignant hyperthermia General features Pathology Pathophysiology Specific causes Myoglobinuria: Acquired causes Muscle activity Overactivity Exercise Drugs Idiopathic recurrent Infections Ischemia (Hypoxia) Compartment syndromes Mitochondrial Neuroleptic malignant syndrome Other: Occasional myoglobinuria Polymyositis: Anti-MAS syndrome Serotonin syndrome Snake venoms Systemic Hypokalemia Thyroid: Hyper or Hypo Toxins Trauma Myoglobinuria: Familial causes Acyl-CoA Dehydrogenase (VLCAD) Carnitine Palmitoyltransferase II (CPT2) Central core Childhood/Juvenile Recurrent COL4A1: HANA

Related Conditions

Shared genes
ACUTE MYOPATHY & NMJ DISORDERS
MASSRPPERIODIC
Ethanol-Induced Myopathies
MAS

External Resources

WUSTL Neuromuscular
Washington University Disease Center
PubMed
Biomedical Literature
GeneReviews
NCBI Expert-Authored Reviews
Orphanet
Portal for Rare Diseases
NORD
National Organization for Rare Disorders

Data sourced from the Washington University Neuromuscular Disease Center. For clinical use, always refer to primary sources.