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(G71.0) Muscular dystrophy
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325 177 in individuals diagnosis muscular dystrophy confirmed
55 116 deaths with diagnosis muscular dystrophy
17% mortality rate associated with the disease muscular dystrophy
Diagnosis muscular dystrophy is diagnosed Men are 28.56% more likely than Women
209 018
Men receive the diagnosis muscular dystrophy
34 857 (16.7 %)Died from this diagnosis.
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116 159
Women receive the diagnosis muscular dystrophy
20 259 (17.4 %)Died from this diagnosis.
Risk Group for the Disease muscular dystrophy - Men aged 5-9 and Women aged 60-64
In Men diagnosis is most often set at age 0-89
Less common in men the disease occurs at Age 90-95+Less common in women the disease occurs at Age 95+
In Women diagnosis is most often set at age 0-94
Disease Features muscular dystrophy
Absence or low individual and public risk
Muscular dystrophy - what does this mean
Muscular dystrophy is a group of inherited muscle diseases that cause progressive weakness and loss of muscle mass. it is caused by mutations in certain genes that are involved in the production of proteins that are essential for muscle health. these mutations cause the body to produce abnormal or missing proteins, which leads to the breakdown of muscle tissue and the eventual weakening of the muscles.
What happens during the disease - muscular dystrophy
Muscular dystrophy is a group of inherited muscle diseases caused by a genetic mutation that affects the production of proteins necessary for normal muscle function. this mutation results in the progressive weakening of the muscles, which can lead to difficulty in walking, climbing stairs, and even breathing. the exact cause of the genetic mutation is unknown, but it is believed to be passed down through families.
Clinical Pattern
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How does a doctor diagnose
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Treatment and Medical Assistance
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23 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Muscular dystrophy - Prevention
Muscular dystrophy is a genetic disorder that cannot be prevented, but there are steps that can be taken to reduce the risk of developing the condition. these include avoiding smoking, maintaining a healthy weight, eating a balanced diet, and engaging in regular physical activity. genetic counseling and testing may also be recommended for those with a family history of the disorder.