Also called: Myopathy
Important: This page is general information, not medical advice. It does not recommend or prescribe any treatment. Always consult your doctor or pharmacist before starting, stopping or changing any medicine.
About Muscle Disorders
Your muscles help you move and help your body work. Different types of muscles have different jobs. There are many problems that can affect muscles. Muscle disorders can cause weakness, pain or even paralysis.
Causes of muscle disorders include:
- Injury or overuse, such as sprains or strains, cramps or tendinitis
- A genetic disorder, such as muscular dystrophy
- Some cancers
- Inflammation, such as myositis
- Diseases of nerves that affect muscles
- Infections
- Certain medicines
Sometimes the cause of muscle disorders is unknown.
It sits within Bones, Joints and Muscles.
The lead U.S. institute for this subject is the National Institute of Arthritis and Musculoskeletal and Skin Diseases.
When to speak to someone. Reading about a topic cannot tell you whether it applies to you. Speak to a doctor or pharmacist if symptoms are severe, sudden, getting worse, or simply not going away — and seek emergency care immediately for chest pain, breathing difficulty, sudden weakness or confusion, or a serious allergic reaction.
Research on Muscle Disorders
13,717 studies areregistered for this condition on ClinicalTrials.gov, the U.S. National Library of Medicine's public registry. A selection is below — the links go straight to the registry entry, not to a summary of ours.
What a registered study does and does not mean. Registration means a study exists and has been declared publicly. It says nothing about whether the treatment being tested works, is safe, or is available to you. Many studies find no benefit — that is what research is for. Never seek out an experimental treatment on the strength of a registry entry alone.
Research currently under way
- Study to Assess the Efficacy and Safety of IMVT-1402 in Participants With Mild to Severe Generalized Myasthenia GravisImmunovant Sciences GmbH
- Effect Of Whole or Skimmed Milk Greek Yogurt on Integrated Muscle Protein Synthesis, Glucose Homeostasis, and Cognition in Post-Menopausal WomenUniversity of Arkansas
- A Real-World Medical Chart Review of Spinal Muscular Atrophy Patients Treated With Onasemnogene Abeparvovec in Saudi ArabiaNovartis Pharmaceuticals
- Mechanism Study of Yangyin Roujin Formula in the Treatment of Fibromyalgia SyndromeJuan Jiao
- FAST for DM - Fatty Acid Supplementation Trial (FAST) for Dermatomyositis (DM)National Institute of Environmental Health Sciences (NIEHS)
- Efficacy, Safety, and Tolerability of Zeleciment Basivarsen (DYNE-101) in Participants With Myotonic Dystrophy Type 1Dyne Therapeutics
Research already completed
- Short-Term Symptom Changes in Adults With Teeth Clenching or Grinding and Jaw Symptoms Receiving Splint, Botulinum Toxin, or Medication Plus Splint CareRecep Tayyip Erdogan University
- Environmental Risk Factors for Myositis in Military PersonnelNational Institute of Environmental Health Sciences (NIEHS)
Study data from ClinicalTrials.gov, a service of the U.S. National Library of Medicine. Retrieved 2026-07-30. Registry entries are supplied by study sponsors and investigators; ClinicalTrials.gov does not verify their scientific validity. PocketsInfo is not affiliated with, and not endorsed by, the NLM or the NIH.
Where to read more
Rather than paraphrase, we point you to the primary sources. Every link below is to a government health agency, a national institute or a recognised medical body — grouped by what you are trying to find out.
Diagnosis and Tests
- Creatine KinaseNational Library of Medicine
- Electromyography (EMG) and Nerve Conduction StudiesNational Library of Medicine
Related Issues
- Foot Drop SyndromeNational Institute of Neurological Disorders and Stroke
Genetics
- Actin-accumulation myopathy: MedlinePlus GeneticsNational Library of Medicine
- Adenosine monophosphate deaminase deficiency: MedlinePlus GeneticsNational Library of Medicine
- Brody myopathy: MedlinePlus GeneticsNational Library of Medicine
- Cap myopathy: MedlinePlus GeneticsNational Library of Medicine
- Central core disease: MedlinePlus GeneticsNational Library of Medicine
- Centronuclear myopathy: MedlinePlus GeneticsNational Library of Medicine
- Collagen VI-related myopathy: MedlinePlus GeneticsNational Library of Medicine
- Congenital fiber-type disproportion: MedlinePlus GeneticsNational Library of Medicine
- Danon disease: MedlinePlus GeneticsNational Library of Medicine
- Early-onset myopathy with fatal cardiomyopathy: MedlinePlus GeneticsNational Library of Medicine
- Fibrodysplasia ossificans progressiva: MedlinePlus GeneticsNational Library of Medicine
- Glycogen storage disease type III: MedlinePlus GeneticsNational Library of Medicine
- Glycogen storage disease type VII: MedlinePlus GeneticsNational Library of Medicine
- Hereditary myopathy with early respiratory failure: MedlinePlus GeneticsNational Library of Medicine
- Hyperkalemic periodic paralysis: MedlinePlus GeneticsNational Library of Medicine
- Hypokalemic periodic paralysis: MedlinePlus GeneticsNational Library of Medicine
- Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia: MedlinePlus GeneticsNational Library of Medicine
- Isolated hyperCKemia: MedlinePlus GeneticsNational Library of Medicine
- KCNK9 imprinting syndrome: MedlinePlus GeneticsNational Library of Medicine
Clinical Trials
- ClinicalTrials.gov: Muscular DiseasesNational Institutes of Health
- ClinicalTrials.gov: RhabdomyolysisNational Institutes of Health
Medical subject headings
Clinicians and researchers index this subject under Muscular Diseases. These are the terms to use when searching medical literature.
This page is built from the MedlinePlus health topic record for Muscle Disorders, a service of the U.S. National Library of Medicine (NLM), National Institutes of Health. Information is from MedlinePlus.gov. PocketsInfo is not affiliated with, and is not endorsed by, the NLM or the NIH. Retrieved 30 July 2026.