Muscular Dystrophy Research Paper

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Muscular dystrophy refers to a group of genetic (inherited) conditions that cause the body's muscles todeteriorate slowly over time, and become increasingly weak. Some of the signs and symptoms ofMuscular dystrophy are: problems with coordination and mobility with frequent falls, muscle weakness, and joint stiffness. High levels of a chemical called creatine kinase (CPK) found in the blood may alsohelp diagnose muscular dystrophy. High levels of creatine kinase don't give a definite diagnosis, sincemany other muscle diseases can also cause this.Testing for very low levels of dystrophin in the muscles such as Duchenne muscular dystrophy, can beused to diagnose muscular dystrophy. For other types of muscular dystrophy, specific blood tests can bedone to help the doctors determine which type of muscular dystrophy a patient have.A test called an electromyogram (EMG) involves passing tiny electrical shocks through the muscles. …show more content…
A muscle biopsy mayalso be used to help with diagnosis. In this procedure, a doctor surgically removes a small piece orsample of the muscle and looks at it under the microscope. A muscle with muscular dystrophy hasmany dead and abnormally large muscle fibres. As the disease progresses, the dead muscle is replacedwith fat and other kinds of tissue.There is no cure for muscular dystrophy, but exercise and physical therapy can keep the muscles fromtightening up around the joints. Assistive devices such as braces and wheelchairs can also help peoplewith muscular dystrophy. People with Duchenne muscular dystrophy can also take a corticosteroidmedication for muscle weakness. Every effort should be made to prevent viral infections that couldprogress to pneumonia. Couples that have a history of muscular dystrophy in their families may want togo for genetic

Muscular Dystrophy Research Paper

There are more than thirty forms of muscular dystrophy. Duchenne Muscular Dystrophy is the most common and serve form among children. It accounts for more than 50% of all cases of muscular dystrophy. Duchenne Muscular dystrophy is a serve form of muscular dystrophy caused by a genetic defection. It is a progressive neuromuscular disorder affecting one in 3600 boys though it is rare for girls to inherit the genetic condition. The genetic disorder targets and causes muscle degeneration and can result…

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Duchenne Muscular Dystrophy Research Paper

Duchenne muscular dystrophy (DMD ) is a muscle disease that includes muscle weakness and can be inherited and can gradually worsen over time. It’s caused by a defective gene and it affects more boys than girls, but the girls can be carriers for the disease. Many young infant males are affected by this disease, and, as time passes, they start to develop symptoms (University of Maryland Medical Center (UMMC), 2014). DMD is a muscular disease that is inherited and causes muscle weakness . What is…

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Becker Muscular Dystrophy Research Paper

Becker Muscular Dystrophy is an inherited genetic disorder, linked to a recessive X-gene. It involves progressive muscle weakness and eventual degeneration. The disorder is caused by a mutated or flawed gene, known as dystrophin, which keeps muscle cells intact. But the genes are shortened, fragile and only partially functional. The mutated genes affect the proper amount of protein that is needed to keep muscles strong and growing. The muscles eventually begin to deteoriate as time progresses, and…

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Duchenne Cerebral Essay

What Is Duchenne Muscular Dystrophy? What Is Duchenne Muscular Dystrophy? DMD is caused by a change in a gene responsible for making the protein dystrophin, which keeps muscles strong and healthy. This change is referred to as a mutation. When there is a mutation in this gene, the protein dystrophin does not work. The muscle cells become weak and they gradually break down. DMD usually affects boys; it is extremely rare in girls. DMD is a progressive disease. At first, the weakness is mostly…

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Video Games and Chiropractors Essay

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