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(G72.8) Other specified myopathies
More details coming soon
349 096 in individuals diagnosis other specified myopathies confirmed
8 471 deaths with diagnosis other specified myopathies
2% mortality rate associated with the disease other specified myopathies
Diagnosis other specified myopathies is diagnosed Men are 5.94% more likely than Women
184 919
Men receive the diagnosis other specified myopathies
4 309 (2.3 %)Died from this diagnosis.
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164 177
Women receive the diagnosis other specified myopathies
4 162 (2.5 %)Died from this diagnosis.
Risk Group for the Disease other specified myopathies - Men aged 60-64 and Women aged 80-84
In Men diagnosis is most often set at age 0-94
Less common in men the disease occurs at Age 95+in in women, the disease manifests at any age
In Women diagnosis is most often set at age 0-95+
Disease Features other specified myopathies
Absence or low individual and public risk
Other specified myopathies - what does this mean
Other specified myopathies are a group of rare muscle diseases caused by genetic mutations that affect the structural and functional integrity of the muscles. these diseases can be inherited or acquired, and can lead to a variety of symptoms such as muscle weakness, pain, stiffness, and wasting. diagnosis is often based on a combination of physical exam, laboratory tests, imaging, and genetic testing. treatment is tailored to the specific myopathy and may include physical therapy, medications, and lifestyle modifications.
What happens during the disease - other specified myopathies
Other specified myopathies is a group of neuromuscular disorders that are characterized by muscle weakness and wasting due to damage to the muscle fibers. the cause of this disorder is not known, however, it is believed to be caused by a combination of genetic and environmental factors. in some cases, other medical conditions, such as metabolic or endocrine disorders, can contribute to the development of the disorder. in addition, the use of certain medications, such as statins, can also increase the risk of developing this condition.
Clinical Pattern
More details coming soon
How does a doctor diagnose
- Medical history and physical examination
- Electromyography (EMG)
- Muscle biopsy
- Genetic testing
- Laboratory tests (e.g. creatine kinase, aldolase, lactic acid)
- Imaging (e.g. MRI, CT scan)
Treatment and Medical Assistance
Main goal of the Treatment: To reduce the symptoms of Other Specified Myopathies.
- Physical therapy
- Occupational therapy
- Medication to reduce muscle spasms and pain
- Corticosteroids to reduce inflammation
- Immunosuppressants to reduce the risk of infection
- Plasma exchange to remove antibodies from the blood
- Surgery to correct deformities
- Nutritional supplements to improve nutrition
- Exercise to improve strength and endurance
- Assistive devices to increase mobility
21 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Other specified myopathies - Prevention
Other specified myopathies can be prevented by avoiding activities that can cause muscle strain, such as lifting heavy objects or participating in contact sports. eating a balanced diet with adequate protein and vitamins, as well as getting enough rest and exercise, can also help to reduce the risk of developing these conditions.