In this assignment you will compare DMD and ALS. Fill in the table below using information from the book and websites. Research at least 2 new therapies for each disease. List the complete URLs of the websites where you found information. |DMD|ALS|Early symptoms|·…
1. Dunchenne muscular dystrophy is a genetic disorder due to progressive weakness and degeneration of muscle cells over time, discovered by Guillaume Duchenne.…
Muscular System: The muscular systems is responsible for maintaining posture, circulating blood, and movement. Visceral muscle is found inside of organs like the stomach, intestines, and blood vessels. The stomach secretes acid and enzymes that digest food. The muscular system also has another variant which is skeletal muscle. The skeletal muscles are attached to bones and move various parts of the body. The biceps, pectoralis major, triceps, nasalis, and deltoid are five major organs in the muscular system. The biceps main job is to control the movement of the elbow and shoulder. The pectoralis major make up most of the chest bulk. The triceps help extend and retract the forearm. The nasalis compress nasal cartilage. The deltoid is responsible…
- duchenne- most common form in children- affects only males; muscles decrease in size and…
Muscular dystrophies are a group of genetic conditions characterized by progressive muscle weakness and wasting (atrophy). The Duchenne and Becker types of muscular dystrophy are two related conditions that primarily affect skeletal muscles, which are used for movement, and heart (cardiac) muscle. These forms of muscular dystrophy occur almost exclusively in males.…
The reason for the request: Ethan and Joshua are brothers that suffer from Duchenne Muscular Dystrophy (DMD). Feel free to go to the official MDA website, click on diseases link then DMD https://www.mda.org/disease/list to learn more about this debilitating, crippling and life threatening disease. As you can imagine, even with Medicaid & SSI caring for two boys with these needs can be tremendous and overwhelming. Unfortunately, when they want things they mostly go without said thing, sometimes even if it benefits them. In this case they both have been wanting their own personal gaming console, like an Xbox One X or Nintendo Switch gaming system. Gaming for them is very important since they are very physically limited.…
Duchenne MD is the most common muscle dystrophy. Due to the way the disease is acquired, it generally influences young men. It is conceivable…
Spinal muscular atrophy [SMA] is a disorder in which, you have a loss of motor neurons. Your muscle symmetry is often off. In addition, there is muscle weakness in your spinal cord. This occurs in a hard time sitting up and holding your head up on your own. It is just like when you are a newborn and you need a pillow to sit on the couch. A few major causes of SMA are loss of motor neuron cells or nerve cell. This mutation leads to a deficiency of motor neuron cells or nerve cells. The disorder SMA is tied to the gene "SMN1" and tied to chromosome 5. A few symptoms of this disorder are- difficulty breathing lack of oxygen, difficulty eating, floppy posture, small amount of movement, and all these symptoms will gradually get worse over time. All these symptoms are at about a mild level in the beginning.…
Duchenne muscular dystrophy also known as DMD is a rare genetic condition that could affects all race and cultures; mostly boys. Duchenne muscular dystrophy affects 1 in 500 boys in approximation. According to muscular dystrophy association 20,000 children are born with DMD worldwide and approximately, 35% are as a result of spontaneous genetic mutation (2014). The disease is an X-linked recessive inheritance that the mother passed it on. DMD has a progressive muscular degeneration and weakness and it is one of the nine types of muscular…
Duchenne muscular dystrophy is a muscular dystrophy but in order to understand it and how it works you will need to know about genetics and how they work and after that, I can tell you about a few treatments and therapies.…
Duchenne Muscular Dystrophy is an X-linked recessive disorder and that’s why it’s more common in males. As for females, they can only be a carrier of the disease and it’s rare for them to experience the symptoms. Put another way, females have two X-chromosomes, so that’s why the disease will not affect them. In female carriers, they would have one defected gene and one normal. That is to say, their normal gene is technically extra for the defected one and will provide the information that is needed. By way of contrast, males can only have one X-chromosome, so that’s why the disease affects males more rather than females.…
Duchenne Muscular Dystrophy is “an X-linked disease of muscle caused by an absence of the protein dystrophin” (Dr. Sussman). The disease affects young boys. If a boy…
Glycogen Storage Disease type III is an autosomal recessive disorder that is caused by the deficiency of the glycogen debrancher enzyme. This deficiency causes there to be a mutation on exon three and it causes abnormally structured glycogen to be present in the body. This disease can be diagnosed by multiple tolerance tests and it also can be diagnosed by analyzing the muscle tissues. This disease causes problems in the liver and in the muscles. The tolerance tests are used to test for liver diseases and the analysis of the muscles is used in order to determine if a patient has myopathy. This disease affects a large range of ages. This ages can range from early childhood to adulthood usually between ages one and sixty-two. Children and adults usually experience different symptoms. The symptoms in children are most commonly growth and muscle retardation. The symptoms in adults usually vary in comparison to children. Adults usually have myopathy in there calf muscles.…
Many men are becoming irritable, tired with energy levels at a all time low and wondering what could be wrong with them. A lot of studies are showing up that Klinefelter 's is what they have. Klinefelter 's Syndrome is a chromosomal disorder that only affects males. A normal male has and X and a Y chromosome in the 23 pair. However, a male with Klinefelter 's Syndrome has an X, Y and another X. “It 's that second X chromosome that causes the signs and symptoms of Klinefelter 's syndrome” (Paulos, 1). Men with Klinefelter 's usually develop more breast tissue than normal, this is called gynecomastia. The most major symptom males experience…
There are about 1,098 human X-linked genes. Most of them code for something other than female anatomical traits. Many of the non-sex determining X-linked genes are responsible for abnormal conditions such as hemophilia , Duchenne muscular dystrophy , fragile-X syndrome , some high blood pressure, congenital night blindness, G6PD deficiency, and the most common human genetic disorder, red-green color blindness. X-linked genes are also responsible for a common form of baldness referred to as "male pattern…