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Genetic counseling is advised when there is a family history of muscular dystrophy. Women may have no symptoms but still carry the gene for the disorder. Duchenne muscular dystrophy can be detected with about 95% accuracy by genetic studies performed during pregnancy.
http://www.nlm.nih.gov/medlineplus/ency/article/001190.htm
http://en.wikipedia.org/wiki/Muscular_dystrophy
What else can I help you with?
Do people with muscular dystrophys kids always have muscular dystrophy?
Not necessarily. Inheritiance of muscular dystrophy is not automatic. Children of a parent with muscular dystrophy have a 50% chance of inheriting the condition, depending on the specific type and genetic pattern of the disease.
Which type of disorder is muscular dystrophy?
Muscular dystrophy is a type of genetic disorder. The disorder weakens the muscles until they can no longer move. People with this disorder do not produce a protein needed for healthy muscles.
What is mixed muscular dystrophy?
Mixed Muscular Dystrophy is a rapid progression form of Muscular Dystrophy. This normally occurs to people between the ages of 30 and 50 and death normally occurs within 5 years.
Is muscular dystrophy and duchenne muscular dystrophy the same?
Muscular dystrophy is a group of genetic disorders characterized by muscle weakening and wasting, while Duchenne muscular dystrophy (DMD) is a specific type of muscular dystrophy caused by mutations in the dystrophin gene. DMD is the most common and severe form of muscular dystrophy, typically affecting boys and leading to progressive muscle weakness and loss of function.
Famous people with duchenne muscular dystrophy?
Duchenne muscular dystrophy is a rare genetic disorder that primarily affects males. Due to the severity of the condition, there are no famous individuals known to have had Duchenne muscular dystrophy.
What percent of people are affected by muscular dystrophy?
1 in 3500 males
What are some statistics about muscular dystrophy?
1 in every 3,500 to 5,000 people in the u.s. get diagnosed
Who muscular dystrophy affects?
MD is a genetic disorders in which strength and muscle bulk slowly weakens. It is caused by incorrect or missing genetic information. Without this information you can not build or maintain healthy muscles. You slowly lose the ability to walk or even sit up right. This disease can occur at any age in a persons life and there is no known cure.
How many people have muscular dystrophy?
Muscular dystrophy encompasses a group of genetic disorders characterized by progressive muscle weakness and degeneration. It is estimated that approximately 1 in 3,500 to 5,000 males are affected by Duchenne muscular dystrophy, the most common form, while other types have varying prevalence. Overall, it's estimated that around 250,000 individuals in the United States are living with some form of muscular dystrophy. Global prevalence varies, but the condition is generally considered rare.
How does muscular dystrophy affect people?
Muscular dystrophy is a group of genetic disorders that lead to progressive weakness and loss of muscle mass. This can result in difficulty with movement, breathing, and other physical functions. The severity of symptoms and progression of the disease can vary depending on the specific type of muscular dystrophy.
What is the oldest age for a person to live with muscular dystrophy?
In most cases this is diagnosed by age five. In that case the child would need a wheelchair by about age 12. Most likely the child will start to have heart and lung issues by late teens or early twenties. My guess no longer than thirty.
How many people in the world have muscular dystrophy?
Approximately 1 in every 3,500 to 5,000 males is affected by muscular dystrophy, depending on the specific type of the disease. This translates to around 250,000 to 300,000 individuals in the United States alone. Globally, estimates suggest that muscular dystrophy affects hundreds of thousands of people, though exact numbers can vary due to factors like underdiagnosis and differing prevalence rates in various regions.
