Muscular Dystrophy Essay

Duchenne Muscular Dystrophy (DMD) is a fatal genetic disorder that is caused by mutations in the gene DMD, which encodes the muscle protein, dystrophin. Dystrophin protein is crucial to preserve the strength, stability, and flexibility of muscle fibers, which protects them from injury as they contract and relax. The DMD gene is primarily located in skeletal and cardiac muscle. Duchenne Muscular Dystrophy is caused by mutations in the gene that produce premature stop codons. The premature stop codons

Duchenne Muscular Dystrophy (DMD) refers to the muscle appearing poorly nourished because of degeneration, which leads to muscle weakness and lost of muscle mass. DMD is a disorder that is caused by genetic mutations in the dystrophin gene. Dystrophin is a muscle that connects the cytoskeleton to the extracellular matrix (ECM). Tidy, D. C. (2016, April 15). When nonsense mutation or frameshift mutation occurs in dystrophin, it results in no protein at all, which causes a severe form of DMD. A dystrophin

Muscular dystrophy is a group of diseases that cause an abnormal progressive deteriorating of the muscles, leading to muscle weakness. Many different types of dystrophy are known, characterized by the muscle groups affected. The disease is caused from a genetic mutation that prevents a protein essential for normal muscle activity from being made, or being produced correctly. In each type of muscular dystrophy, a different protein is irregular (Emery, 2008). Furthermore, because this disease is due

is Muscular Dystrophy? A neuromuscular disease that causes damages to the muscles over time is called muscular dystrophy. This disease is genetically passed down from generation to generation. The cause of the muscle weakness is a lack of protein called dystrophin. This is how they named it muscular dystrophy. This protein causes a numerous of problems for people who have this disease. The disease is only in males, especially the younger male. There are a lot of types of muscular dystrophy. The

Duchenne's muscular dystrophy, also known as psuedohypertrophic muscular dystrophy, is a typical sex-linked disorder in which the muscles degenerate throughout a person's life. It literally means "faulty nutrition of the muscles." Muscular Dystrophy has no cures, and this particular type of muscular dystrophy affects only males. One in 3,500 baby boys are born with this disorder and survival is rare beyond the early 30s, death is usually caused by a respiratory disease. (ygyh.org) Duchenne's

Muscular dystrophy is a lethal sex-linked disorder characterised by progressive muscle weakness and muscle degeneration. It has been a medical problem for many years. In particularly Duchenne muscular dystrophy (DMD) for it is the most frequently occurring and one of the most rapidly progressive in children neuromuscular disorders (MDA, 2015). DMD affects approximately 1 in 3600 live male births throughout the whole world (MDA, 2015). DMD can cause or create an array of difficulties for diagnosed

Ben has a condition called Duchenne Muscular Dystrophy, which is a genetic disease that affects the muscles. A genetic disease is inherited and is explained through the process of DNA, RNA, and cell division. Duchenne has a variety of treatments, but no cures. Muscular Dystrophy, although not common, is a very dangerous condition. The many types can affect the many muscles you have in your body, and can cripple you at a very young age. Even though muscular dystrophy can be diagnosed early, it has no

The first written account of Muscular Dystrophy occurred in 1830, composed by Sir Charles Bell (Audrey S. Penn, 2001). His essay, along with many other accounts, display instances of younger boys getting progressively weaker, losing the ability to walk, and dying at extremely early ages. These diagnostics continued to become more frequent up into the late 1800s and early 1900s. As these symptoms were being researched and observed it soon became prevalent that this disease can affect all people of

to muscular dystrophy and shortening of muscles structures, patient’s mobility can be impaired. Some people will eventually need to use a wheelchair. Additionally, weakened muscles lead to the postural instability resulting in spine curvature disorders. One of the further complications are breathing problems caused by progressive weakness of diaphragm, intercostal and abdominal muscles which are required for proper breathing mechanism. In consequences of those changes patients with muscular dystrophy

similarities between multiple sclerosis and muscular dystrophy. Multiple sclerosis is understood to be an autoimmune disease that affects the central nervous system. However, muscular dystrophy is a genetic disorder that affects the peripheral nervous system. Multiple sclerosis is seen as progressing asymmetrically from the loss of myelin. Likewise, muscular dystrophy presents with a symmetrical wasting of the muscle and distribution of weakness. Muscular dystrophy is a group of similar conditions that