How do muscular dystrophy patients die?
The most common cause of death is heart failure from cardiomyopathy.
Some patients are found to have the genetic abnormalities of the dystrophin gene, but, clinically, have symptoms between those of Duchenne muscular dystrophy (DMD) or Becker muscular dystrophy (BMD)..
Can you get muscular dystrophy at any age?
Muscular dystrophy occurs in both sexes and in all ages and races. However, the most common variety, Duchenne, usually occurs in young boys. People with a family history of muscular dystrophy are at higher risk of developing the disease or passing it on to their children.
Is Muscular Dystrophy life threatening?
Muscular dystrophy is a group of over 30 conditions that lead to muscle weakness and degeneration. As the condition progresses, it becomes harder to move. In some cases, it can affect breathing and heart function, leading to life-threatening complications.
What is the life expectancy of someone with myotonic dystrophy?
The mild form of DM1 is characterized by mild weakness, myotonia, and cataracts. Age at onset is between 20 and 70 years (typically onset occurs after age 40), and life expectancy is normal. The CTG repeat size is usually in the range of 50 to 150.
How old is the oldest person with muscular dystrophy?
The oldest DMD patient he knows is a 54-year-old man in the Netherlands, who had two brothers with Duchenne; one died at 15, the other at 41.
Can muscular dystrophy be cured?
Although there’s no cure for any form of muscular dystrophy, treatment for some forms of the disease can help extend the time a person with the disease can remain mobile and help with heart and lung muscle strength. Trials of new therapies are ongoing.