Muscular Dystrophy Essay

Muscular Dystrophy Scientists have been struggling with the cause, treatment of, and cure for Muscular dystrophy since its discovery in 1886, by Dr. Guillaume Duchenne. Muscular dystrophy is a hereditary disease, affecting thousands of people every year, two-thirds being children between the age of birth through adolescents. Muscular dystrophy can also occur with no family history of the disease. Muscular dystrophy is a degenerating disease, in which the skeletal muscles degenerate, lose their

Muscular Dystrophy When people hear about diseases most of them don’t understand what exactly causes the disease in the first place, or even how widespread it could be. So they go about their days ignoring the disease all together. Such as the case for Muscular Dystrophy (MD). According to the Center for Disease Control (CDC) Muscular Dystrophy in its more predominant forms affects 1 in every 5,000 males. The two most common forms of Muscular Dystrophy, Duchenne and Becker (DBMD), affects 1

shoulders, hips, calves, thighs, pelvic area first. Like other muscular dystrophies, DMD affects the voluntary muscles first and then will progress into other muscles. Limb-girdle muscular dystrophy is another type out of the many that affect voluntary muscles. Specifically, it targets the hips and shoulders. Limb-girdle muscular dystrophy is another disease that causes weakness and wasting of the muscles. Limb-girdle muscular dystrophy (LGMD) is an extremely rare disease that specifically affects

Duchenne Muscular Dystrophy Patients And Carriers.”BMC Neurology 13.1 (2013): 1-7. Academic Search Premier. Web. 15 Dec. 2013 Magee, Justin, Brian McClelland, and John Winder. "Current Issues With Standards In The Measurement And Documentation Of Human Skeletal Anatomy." Journal Of Anatomy 221.3 (2012): 240-251. Academic Search Premier. Web. 16 Dec. 2013. Muscular Dystrophy is a disorder that decreases the function of the body’s muscles and others that control vital organs. Muscular dystrophy means

Duchenne Muscular Dystrophy and Ground-Breaking Research Duchenne Muscular Dystrophy or DMD for short is a genetic disease that affects the skeletal muscles causing muscle degeneration and muscle wasting. Duchenne Muscular Dystrophy is an X-linked recessive chromosomal disease, which is caused by mutations in the DMD Gene (Regenerative Medicine). This Disease affects 1 in 3600 boys (Regenerative Medicine). A male born with this disease experiences respiratory dysfunction, trouble ambulation, cognitive

Description of Muscular Dystrophy. The first record of Muscular Dystrophy (MD) was reported in 1830 by Sir Charles Bell when he wrote a paper about the disease. Symptoms of Muscular Dystrophy: •Difficulty getting up from a lying or sitting position •Walking on the toes •Learning disabilities •Large calf muscles •Frequent falls •Trouble running and jumping All of the symptoms of Muscular Dystrophy are found in males but women can carry the gene but most women aren't affected by it

Muscular dystrophy is not a disease; it’s a term for a genetic mutation. “The disease, mostly affecting males, is transmitted as a sex-linked recessive trait” (Taber’s Cylopedic Medical Dictionary, 2013 pg. 736). There are 9 different types of muscular dystrophy. The two most common types of muscular dystrophy are Duchenne and Becker. “MD is a progressive degeneration of skeletal muscles from an as yet unknown biochemical defect within the muscle” (Sommers, 2011 pg. 691). Males are affected way more

Muscular Dystrophy (MD) is a disease that can be defined as a group of genetic traits that includes deteriorating by the voluntary muscular and/or skeletal movements. Other organs such as the heart are another example of an involuntary muscle that can easily be affected by the disease. Muscular Dystrophy can effect anyone - child or infant, and even middle age to older adults. The overall severity of the disease depends on when it decides to show up. Some factors are simply the age of the individual

Muscular dystrophy is defined as a disease that the causes a loss of muscle mass and progressive weakness. Muscular dystrophy is not and infectious disease, but one that is passed on through abnormal gene mutations that prevent the production of the proteins that are needed to form healthy muscles. Muscular dystrophy is not a single disease, but a group of diseases. There are multiple types of muscular dystrophy, such as Duchenne muscular dystrophy, which is the most common form in male children

Muscular dystrophy (MD) is a genetic neuromuscular disease of various types that all result in the degeneration of muscle issue. The disease manifests in several types that vary by muscular region and dystrophin levels in the body. Most patients with a form of MD will suffer joint and muscle pain, pressure sores, and postural stress due to their condition. Potential clients with this disease will most likely be young boys, as MD mainly affects the male population and shortens one’s life expectancy