Limb-girdle muscular dystrophy life expectancy. Unlike some other forms of muscular dystrophy, this one typically isn’t threatening to heart and breathing function. What is the average life expectancy in duchenne muscular dystrophy? Life expectancy is usually beyond 30s in this type of muscular dystrophy. Learn about prognosis and life expectancy of Duchenne muscular dystrophy, the most common childhood form of the disease, and what factors make living with muscular dystrophy easier. Distal muscular dystrophy is a slow progressing disease. Becker muscular dystrophy has some similarities with Duchenne muscular dystrophy, but is comparatively milder than that. But, as mentioned above, some children are able to live into their 30s or 40s with excellent medical care. The life expectancy for those with this disease is late teens or 20s. They rarely live past twenty to twenty-five years of age. Becker muscular dystrophy. Most of them die in their 20s or early 30s. Walking and sitting often becomes more difficult as the child grows. The life expectancy depends upon the severity of the disease syndrome. People with this type usually live a long life but how long depends on how severe it is and how it progresses. It is characterized by prolonged muscle tensing as well as muscle weakness, pain, and stiffness.Signs and symptoms usually develop during a person's twenties or thirties. Limb-girdle muscular dystrophy is associated with losing the ability to walk between ages 10 and 12. Oculopharyngeal muscular dystrophy (OPMD) is a rare genetic condition. People with limb-girdle muscular dystrophy lose their ability to walk between ages 10 and 12. Becker muscular dystrophy is similar to Duchenne muscular dystrophy… Distal muscular dystrophy life expectancy. shorten life expectancy, and for most people it progresses very slowly, giv-ing you time to prepare for and adjust to changes. The main complications that may reduce the expectation of life are pneumonia and cardiac arrhythmias. Life Expectancy. The average life expectancy is 26 years. The condition may harm vision and cause problems swallowing and talking.  Usually by the age of 12, the child needs a wheelchair because the leg muscles are too weak to work. As with other types of muscular dystrophy, myotonic dystrophy involves progressive muscle weakness and muscle wasting. The type 2 is more common in Finland and Germany. Gene therapy is treatment that may improve the life expectancy for people with DMD much more in future. With medical care, most people with Duchenne MD die from heart or respiratory failure before or during their 30s. Facioscapulohumeral muscular dystrophy generally manifests by the age of 20 years. Patients usually die in their 20s or early 30s. This type also is seen to be affecting only males. Muscular dystrophy is a progressive condition that needs life-long management to prevent deformity and complications. MDA’s research program is constantly making strides toward better treatments and a cure. The life expectancy of someone with Muscular Dystrophy depends on the type that they have because it is different for each type. It usually doesn’t affect a patient’s lifespan. Duchenne MD. Advances in medical management have greatly extended life expectancy for muscular dystrophy. Prognosis & Life Expectancy. Life expectancy is normal but most of the patients will require a wheelchair. The life expectancy of a person suffering from myotonic dystrophy of Steinert is between 15 and 20 years lower than that of the general population. Myotonic dystrophy. Usually people are having normal life expectancy in case of mild syndrome. It causes weakness in the muscles around the upper eyelids and part of the throat called the pharynx. Becker MD. 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