Duchenne muscular dystrophy

children, are affected by the neuromuscular disease Muscular Dystrophy. There are many different types of Muscular Dystrophy and they differ based on which muscles are affected and what the causative protein in the body is. Muscular Dystrophy was first introduced to us in 1830 by Sir Charles Bell, who wrote of an illness that caused a great amount of weakness in young boys. Years later, a French neurologist by the name of Guillaume Duchenne accounted for a small group of boys who had the most…

There are a multitude of different "specific characteristics" for muscular dystrophy. This is because the disease is made up of a multitude of other diseases (roughly 30) that can start as early as childhood. Some will loose the ability to breath or swallow, while others won't be able to walk, however all of those affected by muscular dystrophy will be losing or have weakened muscle mass. The cause of Muscular Dystrophy comes from a defective gene that is most likely inherited but sometimes can…

Muscular dystrophy is a hereditary disease that causes the muscles in your body to weaken, and become wasted. It is a rare disease that affects 20,00 to 200,00 United States citizens per year. It can have life lasting effects on the ones infected. The Department of Medicine/Cardiology, at the University of Minnesota Medical School did a study on prevention for the most common fatal form of muscular dystrophy, Duchenne Muscular Dystrophy. Duchenne Muscular dystrophy is caused by an absence of a…

Duchenne’s muscular dystrophy is a hereditary issue portrayed by dynamic muscle degeneration and shortcoming that happens more in males. It is one of nine sorts of solid dystrophy. DMD quality that can be acquired in families in an X-connected latent style, yet it frequently happens in individuals from families without a known family history of the condition. The quality is the second biggest quality to date, which encodes the muscle protein, dystrophin. Young men with Duchenne solid dystrophy…

first step for a diagnosis is a thorough physical examination by a doctor. Early and overall physical signs of MD will vary due to which specific dystrophy is present. The simplest early physical finding is generalized weakness that starts proximal and spreads distally. An exception is made for a few rare forms of dystrophy such as fasioscapulohumeral dystrophy (FSHD), where symptoms always start at the face accompanied by more distal weakness of extremities 4. Often the examining…

Duchenne’s muscular dystrophy Duchenne’s Muscular Dystrophy Zachary Uecker Genetic Disease Abstract Duchenne’s muscular dystrophy is a genetic disease that targets skeletal muscles and over time, the muscles lose protein and are replaced by fats and connective tissue, making the skeletal muscles unusable. In this paper, the parts of Duchenne’s that will be covered are the method of transmission, statistics about Duchenne’s in the population, the pathophysiology, the body systems…

Myotonic Dystrophy is an autosomal dominantly inherited disorder at which an individual has the inability to relax his or her muscles; thus progressing to muscle degeneration and decrease muscle tone [1]. Currently there are two types of muscular dystrophy that are known in the both the medical and scientific community. There’s type one myotonic dystrophy also known as congenital myotonic dystrophy which has an onset at birth. Then there is type two, myotonic muscular dystrophy which has an…

Everyday people with disabilities are treated unfairly due to their physical appearance. Over the years, having a disability has had a negative stigma within our culture due to the negative labels created by society. Many believe in the ideology that people with disabilities are not able capable of accomplishing the same task as non-disabled people. However, these obstacles have not stopped individuals to advocate for those who are not able to do so. Today they are several laws passed aimed to…

Introduction My task was replicating the experiences a seventeen-year-old male with Becker Muscular Dystrophy (BMD) could encounter. As a part of the experience, the task requires me to consider that BDM is an ailment that the principal effects are characterized by progressive muscle weakness and wasting much like Duchenne (Lister Hill National Center for Biomedical Communications, 2016). BMD is brought on by a X-linked mutations of the dystrophin gene (Mah et al., 2014). The mutation causes…

In class, we’ve talked about the myosin when seeing the microfilament. It is the motor protein of microfilament which moves along it tracks toward the positive end. It is also the major component of skeletal muscle thick filaments and thus, is involved in muscle contraction. The disease that is going to discuss is related to muscle contraction, called Myosin Storage Myopathy (also known as hyaline body myopathy). The characteristic or symptom of this disease is the weakness of the muscles that…