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