Once the heart and respiratory muscles are damaged, Duchenne MD becomes life-threatening. People with limb-girdle muscular dystrophy lose their ability to walk between ages 10 and 12. Patients usually die in their 20s or early 30s. They rarely live past twenty to twenty-five years of age. Gene therapy is treatment that may improve the life expectancy for people with DMD much more in future. The main complications that may reduce the expectation of life are pneumonia and cardiac arrhythmias. People with this type usually live a long life but how long depends on how severe it is and how it progresses. Myotonic dystrophy type 2, one of the two types of myotonic dystrophy, is an inherited muscular dystrophy that affects the muscles and other body systems (e.g., heart, eyes, and pancreas). 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. But, as mentioned above, some children are able to live into their 30s or 40s with excellent medical care. Life Expectancy. Walking and sitting often becomes more difficult as the child grows. The incidence rate is more in Type 1 than the type 2, it has been estimated that 1 in 8000 people suffer from MMD. 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. Life expectancy is normal but most of the patients will require a wheelchair. Facioscapulohumeral muscular dystrophy generally manifests by the age of 20 years. It usually doesn’t affect a patient’s lifespan. Life expectancy is usually beyond 30s in this type of muscular dystrophy. The symptoms start later in life and progress slowly. Prognosis & Life Expectancy. Becker MD. What is the average life expectancy in duchenne muscular dystrophy? Usually people are having normal life expectancy in case of mild syndrome. This type also is seen to be affecting only males. Limb-girdle muscular dystrophy life expectancy. Usually by the age of 12, the child needs a wheelchair because the leg muscles are too weak to work. 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. shorten life expectancy, and for most people it progresses very slowly, giv-ing you time to prepare for and adjust to changes. Distal muscular dystrophy life expectancy. Duchenne MD. As with other types of muscular dystrophy, myotonic dystrophy involves progressive muscle weakness and muscle wasting. Becker muscular dystrophy is similar to Duchenne muscular dystrophy… The life expectancy for those with this disease is late teens or 20s. Advances in medical management have greatly extended life expectancy for muscular dystrophy. Oculopharyngeal muscular dystrophy (OPMD) is a rare genetic condition. The type 2 is more common in Finland and Germany. Unlike some other forms of muscular dystrophy, this one typically isn’t threatening to heart and breathing function. MDA’s research program is constantly making strides toward better treatments and a cure. It causes weakness in the muscles around the upper eyelids and part of the throat called the pharynx. The average life expectancy is 26 years. The condition may harm vision and cause problems swallowing and talking.  Most of them die in their 20s or early 30s. Becker muscular dystrophy. Distal muscular dystrophy is a slow progressing disease. The life expectancy depends upon the severity of the disease syndrome. Becker muscular dystrophy has some similarities with Duchenne muscular dystrophy, but is comparatively milder than that. With medical care, most people with Duchenne MD die from heart or respiratory failure before or during their 30s. 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