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