Duchenne Muscular Dystrophy Essay

Duchenne Muscular Dystrophy What is the Duchenne Muscular Dystrophy? Duchenne Muscular Dystrophy is a sex-linked disease, which is inherited in a recessive fashion (National Human Genome Research Institute, 2013). Over thirty similar genetic disorders exist (Duchenne Foundation Australia, 2015). All types of muscular dystrophy are considered to be a rare disorder (Duchenne Foundation Australia, 2015). Duchenne Muscular Dystrophy is most common in children and causes muscle weakness and wasting, which

1. Duchenne Muscular Dystrophy is one of the nine types of muscular dystrophy and the most known, it’s a genetic disorder distinguish by ongoing muscle degeneration and weakness. DMD is cause by a mutation on the X chromosome that stops the production of dystrophin, which is a normal protein in muscles. 2. The typical microscopic changes in the muscle changes noted in the muscle tissue of someone with Duchenne muscular dystrophy is the muscle fibers are darker and denser than usual, there is a

Duchenne muscular dystrophy, classified as a genetic disorder, is marked by progressive muscle degeneration and weakness. It is only one of the nine forms of muscular dystrophy; however, around half of the people diagnosed with muscular dystrophy have Duchenne muscular dystrophy. Each strain of muscular dystrophy is created by a genetic mutation distinct to that type. Duchenne’s has an absence of dystrophin, a protein that aids in keeping muscle cells together. Most of the mutations in the genes

Case Study – Muscular Dystrophy 1. The meaning of Duchenne muscular dystrophy is a severe form of muscular dystrophy caused by a genetic defect that can be characterized by a disturbed growth of cardiac and skeletal muscles. It usually affects boys. In 1861, a French neurologist, Guillaume B. Duchenne, was the first person to give a detailed description of this syndrome. 2. The typical microscopic changes noted in the muscle tissue of someone with Duchenne’s muscular dystrophy is degenerating skeletal

Inheritance Duchenne muscular dystrophy (DMD) is a genetic disease that weakens one’s muscles. DMD is inherited through an X linked pattern due to the gene carrying the DMD mutation is on the X chromosome. The male population are affected by DMD almost exclusive. There is a one in two chance that a male offspring will have DMD if their mother is a carrier of the mutated gene. Every boy inherits an X chromosome from their mother and a Y from their father. If a boy inherits the mutated gene, then they

Duchenne Muscular Dystrophy-Outline Persuasive Presentation Problem-Solution-Visualization Amber Klinkhammer Introduction I. Attention Getter: Many young boys lives are slipping away from them, being claimed by one selfish disease called Duchenne Muscular Dystrophy, while FDA officials in the U.S. stand back and watch it happen. II. Listener Relevance: Duchenne Muscular Dystrophy (DMD), is more common than people think and chances are sooner or later you will know of or see somebody affected

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

Most people probably wonder why this is such a big deal. Once the puzzle piece is on the ground I can’t pick it up. Why is this a problem? It’s a problem because I have Duchennes Muscular Dystrophy and I am in a wheelchair. D.M.D causes muscle weakness. Here is an example of my everyday with Duchennes Muscular Dystrophy. My day starts with a quick look at my phone, it is 5:00 in the morning my back is cramping and I need to be turned on my side. I knock on the wall to get my mom’s attention

Duchenne muscular dystrophy is a genetic disease that pertains only to males caused by a defective gene and normally leads to many problems affecting a child’s leg movement. This disease got its name from the neurologist, Guillaume Benjamin Amand Duchenne. He was a very consistent doctor who followed many patients medical records. He diagnosed one of his patients with muscular dystrophy and then the disease picked up his name, due to his founding. The cause of Duchenne muscular dystrophy is by a

Hey there Zach! I remember replying to a few of your posts last semester. Did you know Duchenne Muscular Dystrophy affects more boys than girls? Expect them to be in a wheel-chair at around during their early teens. It is also know that it takes longer for them to start walking, which means they barely walk during their lives. They even have a hard time raising their arms and fall often if they were walking. They might struggle to climb up the stairs or it may not even be worth the trouble. The