Muscular dystrophy symptoms

Help Fund Advancements in Science and Care for People Living with Neuro muscular Disease. Make a Donation and Give Strength to the People Who Need it the Most! What are the first signs of muscular dystrophy?

How do you know if you have muscular dystrophy? Why does DMD affect mostly boys?

Who treats muscular dystrophy? Muscular dystrophy is a group of diseases that cause progressive weakness and loss of muscle mass. In muscular dystrophy, abnormal genes (mutations) interfere with the production of proteins needed to form healthy muscle. There are many different kinds of muscular dystrophy. Symptoms of the most common variety begin in childhoo mostly in boys.

Becker muscular dystrophy is like Duchenne, except milder. Myotonic muscular dystrophy is the most common form in.

Learn the symptoms , types, and treatment. The disorders differ in which muscles are primarily affecte the degree of weakness, how fast they worsen, and when symptoms begin. While there are fewer than 200cases in the United States, as of right now, there is no cure. Most forms of this serious disease occur in young children, primarily boys. But treatment can help prevent or reduce problems in the joints and spine to allow people with muscular dystrophy to remain mobile as long as possible.

All types cause muscle weakness, but the areas affected and the severity of the symptoms are different. Muscular Dystrophy UK provides a dropdown list of specific muscle-weakening conditions. Other symptoms may include: Muscle weakness that starts in the pelvis, shoulders. Signs and Symptoms What happens to someone with distal muscular dystrophy (DD)? Typically, the first symptom of distal muscular dystrophy (DD) is weakness in the distal muscles — those farthest away from the hips and shoulders such as those in the hands, feet, lower arms or lower legs.

Types of muscular dystrophy include: Duchenne dystrophy — This is the most severe type of muscular dystrophy. It is also the most common. Different types of muscular dystrophy may affect different muscle groups. Patients often have difficulty walking and may have problems with muscle control in other.

Facioscapulohumeral muscular dystrophy (FSHD) is a neuromuscular disease characterized by progressive muscle weakness. The name of this particular type of muscular dystrophy identifies the muscles that are most affected by the disease, those being in the face (facio), back (scapula), and upper.

As the condition progresses, it becomes harder to move. In some cases, it can affect breathing. Oculopharyngeal muscular dystrophy is a genetic disease distinguished by the onset of ptosis, dysphagia, and weakness of voluntary skeletal muscles in elderly individuals. Choking, food regurgitation, and possibly life-threatening aspiration pneumonia are rare but important complications. Symptoms are muscle weakness, shortness of breath, and fatigue.

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 accuracy by genetic studies done during pregnancy.

This deterioration is due to the death of the muscle cells and muscle tissues and leads to ongoing muscle wasting and muscle weakness.