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