In addition the student should have an extra set of books for home to allow him not to have to take them back and forth. This enables the development of certain preventive…… Words: 1509 Length: 4 Pages Document Type: Essay Paper : 5673961 Sister's Keeper Edward and Susan: My Sister's Keeper ethical dilemma The film My Sister's Keeper is an emotionally wrought dramatization of what is a very real medical conundrum for some parents today, given advances in medical technology. The skeleton supports the body, protects internal organs, serves a point of attachment for skeletal muscles for body movement, procedures blood cells, and stores minerals. All the diversity that is observed currently in plant and animal kingdom can be ascribed to evolution over a long period of time. Therefore, lack of any of the proteins of the complex will lead to pathology, resulting in muscle wasting. Genes make humans dynamic organisms capable of development, growth and change.
Fifth, medical experts advice that patients suffering from Muscular Dystrophy should avoid complete inactivity since this will make the condition much worse Kantor, 2006. High frequency oscillatory ventilation in burn patients with the acute respiratory distress syndrome. Phenotype is the specific characteristics that are displayed by the organism. This occurs due to mixture of hypertrophy, atrophy, and necrosis muscle cells. Genes control the nervous system cells, and re-growth of skin and hair cells. A dystrophy is when an organ or tissue in the body wastes away dictionary, 1. They all cause muscle weakness and muscle loss.
Dystrophinopathic diseases are muscular dystrophies that are of a genetic nature caused by a deficiency in the protein dystrophin. This paper provides an analysis of this leadership style drawing on charismatic leadership theory and some of the traits and behaviors of Kelleher that are characteristic of this type of leadership. There are also a few medications that can help relieve pain and stiffness in the muscles. The gene that is responsible for this disorder has been identified on the short arm of the X-chromosomes. Controversy to this, the wheelchair also has disadvantages. Words: 4492 Length: 12 Pages Document Type: Essay Paper : 61564004 living things are characterized by the following seven characteristics namely mobility, respiration, excretion, sensitivity or response to external stimulus, growth, feeding, and reproduction.
It is an annual Labor Day tradition and has been for many decades. The normal body temperature is between 98. Exon skipping prevents the transcription of the exon containing the mutation. The restriction is grounded in the belief that the embryo is a potential human being from the moment of conception. Introduction Duchenne muscular dystrophy is an inherited condition that leads to muscle weakness and progressive degeneration.
Current level of performance The student who is a 13 year old male is a very enthusiastic and happy boy who loves to read, be around people, and listen to music. Muscular dystrophy is a hereditary disease, affecting thousands of people every year, two-thirds being children between the age of birth through adolescents. Ongoing therapy, including , , , and the use of orthopedic instruments, such as wheelchairs and standing frames, are helpful in helping individuals with mobility. Gale Encyclopedia of Medicine, Gale Research, 1999. The trait for muscular dystrophy may be transmitted as an autosomal dominant. Other signs of Duchenne Muscular Dystrophy include muscle wasting and cardiomyopathy. Activities that encourage and maintain movement are suggested as treatment.
Individuals diagnosed with Duchenne Muscular Dystrophy are muscle weaknesses beginning with the legs and pelvis, but may spread to the arms and back, difficulty with gross-motor skills, frequent falls, and fatigue. However, how severe it is dwells on the kind of Muscular Dystrophy suffered from by the patient Kantor, 2006. Allowing the student to participate in all assignments is rewarding, as well as educational. Dystrophin protein normally helps maintain the integrity of the muscle cells. Therefore, there is no difference between phenotypes and are usually influenced by several gene pairs while the environment has a significant influence on the trait. The risk of having an affected child, within the general population, is about 1 in every 3500 male births. Muscular dystrophy research papers examine the medical condition and explicate it fully.
This enables the patient to do some of the things on his or her own, for instance, moving around etc Kantor, 2006. This form of muscular dystrophy is inherited and is caused by a genetic mutation that affects the dystrophin proteins of the muscles. Beth Israel Deaconess Medical Center. While gene based interventions can correct the mutations, pharmacology can prevent future damage and degeneration of muscular functioning. This paper will discuss the basic science that underlies genetic screening, applications of genetic screening, and investigate some of the common misconceptions and ethical questions about its use. The reason we need courage is to keep belief alive. This disorder is caused my mutations in the dystrophin gene.
Muscular dystrophy is a degenerating disease, in which the skeletal muscles degenerate, lose their strength, and cause increasing disability and deformity. Years later, a French neurologist by the name of Guillaume Duchenne accounted for a small group of boys who had the most… Description of the Disorder Duchenne muscular dystrophy is a genetic disorder that is characterized by progressive muscle degeneration and weakness. My father is afflicted with this horrific disease. Usually those affected will not live past the age of… Words 472 - Pages 2 What Is Duchenne Muscular Dystrophy? Human Molecular Genetics, 11 20 , pp. The mundane by excellent cinematography and an effective cast.