People with Duchenne and Becker muscular dystrophy may survive into their 40s or beyond If the cardiac aspects of the disease are minimal, or if they are adequately controlled through medical intervention, a normal or nearly normal life span can be expected. Becker muscular dystrophy has some similarities with Duchenne muscular dystrophy, but is comparatively milder than that. A good control of the disease, going to the medical reviews of the different specialists can improve the life expectancy and reduce the complications associated with … The average life expectancy is 26; however, with excellent care, some may live into their 30s or 40s. The symptoms start later in life and progress slowly. Muscular Dystrophy Association, I had a wonderful childhood. Patients usually die in … Weakness first develops in the hips, pelvis, thighs and shoulders, and people with BMD may have thick calf muscles. This type also is seen to be affecting only males. Most people with Becker muscular dystrophy survive well into mid- to late adulthood. Becker muscular dystrophy (BMD) is an inherited condition that causes progressive weakness and wasting of the skeletal and cardiac (heart) muscles. Life expectancy for muscular dystrophy depends on the type. It was also found that the life expectancy of patients born from 1970 (mostly with ventilatory assistance) was 40.95 years old from 1970 and 25.77 years old before 1970. It is the most common type of muscular dystrophy. Becker : Becker MD is similar to Duchenne, but has a milder effect on muscle movement and appears in people aged anywhere from 5 to 60 years. The life expectancy depends upon the severity of the disease syndrome. The type 2 is more common in Finland and Germany. Usually people are having normal life expectancy in … Life expectancy can reach into the early thirties. Becker muscular dystrophy symptoms Duchenne and Becker muscular dystrophy. Life expectancy is normal but most of the patients will require a wheelchair. It primarily affects males. Becker muscular dystrophy life expectancy. I graduated from college, and I’m now work-ing in L.A. in the television industry. Some children with severe muscular dystrophy may die in infancy or childhood, while adults who have forms that progress slowly can live a normal lifespan. I hope you can tell from my story that having limb-girdle muscular dystrophy The incidence rate is more in Type 1 than the type 2, it has been estimated that 1 in 8000 people suffer from MMD. Muscle weakness usually becomes apparent between the ages of 5 … The different types of the disease vary in the age which muscle wasting becomes manifest and in the muscle groups first affected. Facioscapulohumeral muscular dystrophy generally manifests by the age of 20 years. The age of onset and rate of progression can vary. I use a wheelchair or scooter part time to help me when I work, travel and have fun with my friends. The main complications that may reduce the expectation of life are pneumonia and cardiac arrhythmias. 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. Further, over the years, causes of death also have changed in people with DMD. Contrary to the wide spread notion that muscular dystrophy is exclusively a childhood disorder, clinical onset may occur at any point in the life span. 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. Weakness first develops in the muscle groups first affected depends upon the severity of disease. The muscle groups first affected upon the severity of the disease vary in the age of onset and of... 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