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ACUTE MYOPATHY & NMJ DISORDERS

Neuropathy (Hereditary)
W
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time/nmacute.htm#ACUTE MYOPATHY & NMJ DISORDERS

Overview

From WUSTL Neuromuscular

Myasthenia Gravis Carnitine Deficiency Myoglobinuria/ Rhabdomyolysis Myositis variants: anti-MAS; anti-SRP Periodic Paralysis Myosin deficiency myopathies Electrolyte disorders Potassium: High or Low Magnesium: High PO4: Low Barium: Hypokalemic; External link

Related Conditions

Shared genes
Ethanol-Induced Myopathies
MAS
Muscle Fiber Pathology
VPSRPVAMP
MYOGLOBINURIA - RHABDOMYOLYSIS
MAS
Other Muscle Features
VAMPINCLUSIONBCIM

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.