Muscle diseases refer to various disorders that affect the function of muscles. These diseases can occur as a result of genetic mutations, autoimmune reactions, infections, metabolic disorders, or other factors. Muscle diseases are characterized by symptoms such as muscle weakness, muscle twitching, muscle cramps, muscle pain, and decreased muscle mass and mobility.
Muscle diseases can have various causes.
The diagnosis of muscle diseases involves a detailed neurological examination considering the patient's symptoms and medical history. During the neurological examination, muscle strength, reflexes, muscle tone, and mobility are tested. Blood tests may be used to evaluate the levels of muscle enzymes or detect genetic mutations. Electromyography (EMG) and nerve conduction tests are used to evaluate nerve and muscle functions. Tests such as muscle biopsy and genetic testing may also be used in the diagnostic process.
The treatment of muscle diseases varies depending on the underlying cause, the severity of symptoms, and the patient's condition. In some muscle diseases, supportive treatments are used to alleviate symptoms and improve quality of life. These treatments may include physical therapy, muscle strengthening exercises, respiratory therapy, nutritional support, and rehabilitation. In some cases, medications may be used to increase muscle strength or control symptoms. In genetic muscle diseases, gene therapy or gene editing treatments may be promising in the future. There is no specific treatment for each muscle disease, but there are treatment options available for managing symptoms and improving quality of life.