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    Home > Symptoms of muscular dystrophy

    Symptoms of muscular dystrophy

    • Last Update: 2020-04-03
    • Source: Internet
    • Author: User
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    Muscular dystrophy, also known as muscular dystrophy, has many different types This is a hereditary disease in which muscles gradually weaken and eventually lose weight Learning to recognize the symptoms of muscular dystrophy can help to identify problems at an early stage and increase opportunities for treatment and intervention If there is a family history, it is particularly important to observe early symptoms Many children whose parents suffer from muscular dystrophy develop normally in childhood But as you grow older, signs of muscle weakness begin to appear, such as increased fatigue, difficulty standing and walking, and shaking Patients will often fall down, poor gait (such as walking with toes) and other muscular dystrophy symptoms In the progressive course of muscular dystrophy, the patient will also have muscle enlargement, drooping eyes, face and face, and dyspnea Some patients do not show signs of muscle atrophy until puberty or adulthood, and are usually in a milder form Others begin to show early symptoms in infancy After a period of time, the patient may lose walking ability, experience severe atrophy caused by muscle spasm around the joint, and thus reduce the range of activity of the patient The disease is most common in boys because of its X-linked characteristics X-linked features indicate that boys inherit defective copies of the X chromosome and that the Y chromosome does not have a genetic material to balance defective genes Women can also be carriers of muscular dystrophy, but often don't develop it because they need two defective X chromosomes But depending on the form of carrying, some women also show mild symptoms of muscular dystrophy If the child is found to have symptoms of muscular dystrophy, the doctor will make a blood creatine kinase test to further confirm the diagnosis If the test results show abnormalities, doctors may recommend using genetic tests to determine the specific form of the disease This information is important to identify appropriate treatment measures and long-term plans Appropriate treatment can fundamentally change the quality of life and independent ability of patients, and can potentially prolong the life of patients.
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