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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.
Can people with muscular dystrophy have healthy children?
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
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.
Whan do symptoms of Emery-Dreifuss muscular dystrophy egin?
This type of muscular dystrophy usually begins in early childhood, often with contractures preceding muscle weakness. Weakness affects the shoulder and upper arm originally, along with the calf muscles, leading to foot-drop
When do the symptoms of Becker muscular dystrophy usually appear?
usually appear in late childhood to early adulthood. Though the progression of symptoms may parallel that of DMD, the symptoms are usually milder and the course more variable
How can you spot muscular dystrophy?
Muscular dystrophy may present with symptoms such as muscle weakness, poor coordination, progressive muscle wasting, and difficulty with tasks that require muscle strength. A diagnosis typically involves a physical examination, genetic testing, and muscle biopsy to confirm the condition. If you suspect someone has muscular dystrophy, it's important to consult a healthcare professional for an accurate diagnosis and appropriate management.
A recessive gene located on the X chromosome is the cause of muscular dystrophy in affected individuals. Males are more likely to suffer from muscular dystrophy than females because?
males have only one X chromosome, so if they inherit the gene for muscular dystrophy on that X chromosome, they will develop the disorder. Females have two X chromosomes, so they would need to inherit the gene on both chromosomes to be affected, making it less likely for them to show symptoms.
Can Females get Duchenne's muscular dystrophy?
Yes, there have been documented cases of females getting DMD but it is very rare since the father that affected by the disease must procreate with a female carrier of the disease and create a daughter of course.
What are symptoms or effects of muscular dystrophy?
In the mild form, persons usually develop cataracts and experience mild muscle tone dysfunction (myotonia). They normally do not experience clinical manifestations until they reach 20 years of age
What are some symptoms of the muscular system?
The muscular system doesn't have "symptoms." The muscular systems is just there, and does not have any symptoms.
How can you get Muscular Dystrophy?
There is no known cure for muscular dystrophy, although Eastern philosophies believe that humans can heal many illnesses and conditions by "balancing" the body.In Muscular Dystrophy, prolonged inactivity (such as bed rest and even sitting for long periods) can worsen the disease. Physical therapy, occupational therapy, orthotic intervention (e.g., ankle-foot orthosis), speech therapy and orthopedic instruments (e.g., wheelchairs and standing frames) may be helpful.Occupational therapy assists the individual with MD in engaging in his/her activities of daily living (self-feeding, self-care activities, etc.) and leisure activities at the most independent level possible
What does the diagnosis of muscular dystrophy involve?
a careful medical history and a thorough physical exam to determine the distribution of symptoms and to rule out other causes. Family history may give important clues, since all the muscular dystrophies are genetic conditions
