Muscular Dystrophy Essay

Myotonic Muscular Dystrophy (MMD) Myotonic Muscular Dystrophy, abbreviated MMD, is a disease that affects the muscles and organs of a body. To break Myotonic Muscular Dystrophy down, the word myotonic is the adjective for myotonia, which is an inability to relax muscles at will. Muscular dystrophy means the gradual muscle degeneration, which weakens and shrinks muscle tissue. Knowing the breakdown of MMD, this disease summed up means a person is restricted to relax their muscles at their own will

Topic Paper: Duchenne Muscular Dystrophy Duchenne Muscular Dystrophy is an X-linked genetic disorder caused by a genetic mutation in the dystrophin gene. The disorder is recessive, therefore males are more at risk for displaying the mutation than women. However, women can be carriers and have mild effects. Duchenne Muscular Dystrophy affects the neuromuscular systems, which can result in deterioration of muscles and eventually death.1 The disorder usually presents itself in early childhood, and can

with Duchenne Muscular Dystrophy (DMD) is the prevalence of fibrosis that occurs in the skeletal muscles, heart, and lungs of these patients. In the heart and lungs, fibrosis inhibits the body’s ability to perform cardiopulmonary or respiratory function, respectively. These conditions typically result in death if no emergency medical attention is given. Fibrosis can also present as contractures in the skeletal muscle fibers, which will usually result in the loss of skeletal muscular function and the

Overview: Muscular dystrophy (MD) is a rare, progressive disease relating to the weakening of skeletal muscles. There are more than 30 types of muscular dystrophy that are further divided into nine categories. Duchenne MD is the most common and acute form of this condition that accounts for 50% of all the cases. Duchenne MD (DMD) is most prevalent in males, between the ages of 3 and 5 (Norwood, FL, et al. 2009). This X-linked disease occurs for 1 in every 3,500 males, which results in confinement

Duchenne’s Muscular Dystrophy Duchenne’s muscular dystrophy (DMD) is a progressive genetic disorder that leads to muscle atrophy and eventually death. Diagnosing DMD consists of blood tests, genetic testing, and muscle biopsies. Signs and symptoms begin presenting in toddlers with DMD and progressively worsen throughout life. There is no cure for DMD, and will cause terminal cardiopulmonary complications. Medical interventions consist of corticosteroid treatment, respiratory management, cardiac

Muscular Dystrophy The topic I chose is muscular dystrophy as a muscular disease, when we break the word down into word parts, muscul/o means muscle, -ar means pertaining to, dys- means abnormal and, -trophy means development. Muscular dystrophy is Inherited disease causing a progressive muscle degeneration,weakness, and atrophy. There are many different kinds of muscular dystrophy. They all cause muscle weakness and muscle loss. In muscular dystrophy, abnormal genes interferes with the production

Muscular dystrophy develops weaker and less muscular mass in a category of diseases. Our healthy muscles need more formulation of proteins. Therefore, this only transpires when genes are imperfect. There are nine major types of muscular dystrophy, which include duchenne, becker, congenital, limb-girdle, facioscapulohumeral, emery-dreifuss, distal, myotonic, and oculopharyngeal. Distinguish decay and reconstruction of the muscle fibers, making the skeletal muscle and muscle proteins weaker. Additionally

Causes, Pathogenesis and Outcomes for Duchenne Muscular Dystrophy Introduction Muscular dystrophy is a genetic disorder that causes progressive deterioration of muscles. This essay is going to focus on Duchenne Muscular Dystrophy (DMD) as it is the most common type of muscular dystrophy in Australia and throughout the world. It is also one of the most severe forms, with many patients in wheelchairs by their mid-teens (Muscular Dystrophy Foundation, 2014). It is estimated that DMD affects 1 in 5000

Duchenne muscular dystrophy is an X-linked recessive form of muscular dystrophy, which only affects boys. In the article titled “Timed Rise from Floor as a Predictor of Disease Progression in Duchenne Muscular Dystrophy: An Observational Study”, their purpose for doing this article was to investigate the effect of the time to rise from the floor test on the changes that were observed on the 6 minute walk test (6MWT) over a time period of 12 months. There were 215 boys with this disease that participated

Becker muscular dystrophy (BMD) is a less severe variant of Duchenne muscular dystrophy. Survival is usually into old age. It affects mainly boys, with extremely rare exceptions. I am one of the rare female exceptions to this disease. I was fitted with braces shortly after diagnoses; these aren’t