Duchenne MD. It usually doesn’t affect a patient’s lifespan. The condition may harm vision and cause problems swallowing and talking.  Limb-girdle muscular dystrophy is associated with losing the ability to walk between ages 10 and 12. Life expectancy is usually beyond 30s in this type of muscular dystrophy. Muscular dystrophy is a progressive condition that needs life-long management to prevent deformity and complications. Usually people are having normal life expectancy in case of mild syndrome. Most of them die in their 20s or early 30s. Distal muscular dystrophy life expectancy. The average life expectancy is 26 years. 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. The type 2 is more common in Finland and Germany. The life expectancy for those with this disease is late teens or 20s. They rarely live past twenty to twenty-five years of age. Patients usually die in their 20s or early 30s. Becker MD. 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. Becker muscular dystrophy has some similarities with Duchenne muscular dystrophy, but is comparatively milder than that. Advances in medical management have greatly extended life expectancy for muscular dystrophy. Myotonic dystrophy. Oculopharyngeal muscular dystrophy (OPMD) is a rare genetic condition. 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). Becker muscular dystrophy. Usually by the age of 12, the child needs a wheelchair because the leg muscles are too weak to work. Once the heart and respiratory muscles are damaged, Duchenne MD becomes life-threatening. The symptoms start later in life and progress slowly. Facioscapulohumeral muscular dystrophy generally manifests by the age of 20 years. Limb-girdle muscular dystrophy life expectancy. With medical care, most people with Duchenne MD die from heart or respiratory failure before or during their 30s. Prognosis & Life Expectancy. Walking and sitting often becomes more difficult as the child grows. The main complications that may reduce the expectation of life are pneumonia and cardiac arrhythmias. 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. The incidence rate is more in Type 1 than the type 2, it has been estimated that 1 in 8000 people suffer from MMD. Life expectancy is normal but most of the patients will require a wheelchair. Life Expectancy. It causes weakness in the muscles around the upper eyelids and part of the throat called the pharynx. Gene therapy is treatment that may improve the life expectancy for people with DMD much more in future. 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? But, as mentioned above, some children are able to live into their 30s or 40s with excellent medical care. Distal muscular dystrophy is a slow progressing disease. 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. 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. People with limb-girdle muscular dystrophy lose their ability to walk between ages 10 and 12. The life expectancy depends upon the severity of the disease syndrome. 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