Myopathic changes; Myopathy; Muscle problem
A muscle disorder includes patterns of weakness, electromyogram (EMG) findings, or biopsy results that suggest a muscle problem. The muscle disorder can be inherited, such as muscular dystrophy, or acquired, such as alcoholic or steroid myopathy.
The medical name for muscle disorder is myopathy.
The main symptom is weakness.
Other symptoms include cramps and stiffness.
Blood tests sometimes show abnormally high muscle enzymes. If a muscle disorder might also affect other family members, genetic testing may be done.
When someone has symptoms and signs of a muscle disorder, tests such as an electromyogram, muscle biopsy, or both can confirm whether it is a myopathy. A muscle biopsy examines a tissue sample under a microscope to confirm disease. Sometimes, a blood test to check for a genetic disorder is all that is needed based on someone's symptoms and family history.
Treatment depends on the cause. It usually includes:
Your health care provider can tell you more about your condition and treatment options.
Borg K, Ensrud E. Myopathies. In: Frontera WR, Silver JK, Rizzo TD, eds. Essentials of Physical Medicine and Rehabilitation: Musculoskeletal Disorders, Pain, and Rehabilitation. 3rd ed. Philadelphia, PA: Elsevier Saunders; 2015:chap 135.
Selcen D. Muscle diseases. In: Goldman L, Schafer AI, eds. Goldman-Cecil Medicine. 25th ed. Philadelphia, PA: Elsevier Saunders; 2016:chap 421.
Review Date: 11/22/2017
Reviewed By: Luc Jasmin, MD, PhD, FRCS (C), FACS, Department of Surgery at Providence Medical Center, Medford, OR; Department of Surgery at Ashland Community Hospital, Ashland, OR; Department of Maxillofacial Surgery at UCSF, San Francisco, CA. Review provided by VeriMed Healthcare Network. Also reviewed by David Zieve, MD, MHA, Medical Director, Brenda Conaway, Editorial Director, and the A.D.A.M. Editorial team.
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