Muscular Dystrophy Essay

In this article, the authors discussed the different types of Congenital Muscular Dystrophy: Fukuyama Congenital Muscular Dystrophy, Muscle Eye Brain disease, and Walker Warburg Syndrome. Congenital muscular dystrophies tend to be less common than other muscular dystrophies. Patients that are diagnosed with Congenital muscular dystrophy show symptoms before they are even born. Most rarely move in the womb, due to neonatal hypotonia. Neonatal hypotonia is known as “floppy baby syndrome”, in which

Becker muscular dystrophy (BMD) is an x-linked recessive inherited disorder characterized by slowly progressive muscle weakness of legs and pelvis. This disease primarily effects voluntary muscles such as muscles of the hips, pelvic area, thighs and shoulders. Since this disease effects all your muscles they’d weaken your heart as well. Most people with BMD often develop cardiomyopathy ( disease in the heart muscle). The heart muscle deteriorates like the skeletal and smooth muscles which would

Ben has Duchenne Muscular Dystrophy (DMD). DMD is a degenerative disease of the muscles. When someone has this disease their muscles do not produce enough dystrophin to stay together. This causes the muscles to deteriorate over time. With proper care, the rate of muscle degradation can be slowed down. Duchenne muscular dystrophy is a genetic disorder characterized by progressive muscle degeneration and weakness. Muscle weakness can start as early as age three. It first affects the hips, pelvic area

Becker muscular dystrophy is a degenerative muscular disorder mainly affecting the voluntary muscles. This disease was named after the doctor who discovered it in the 1950s. BMD as it is called, affects the heart but not a severely as Duchenne muscular dystrophy. The symptoms of BMD usually start to affect the person during late childhood and adolescence. The first symptoms start with weakness in the legs and pelvis area , as well as the shoulders. It also affects the heart as the myocardium layer

OTH604 DIAGNOSIS FACT SHEET Muscular Dystrophy DIAGNOSIS: Muscular Dystrophy is a group of diseases that cause progressive weakness and loss of muscle mass. DESCRIPTION: • X- Linked recessive pattern passed on by mother to son • Nine major forms of muscular dystrophy: o Myotonic: most common form of muscular dystrophy in adults. Usually appears any time from early childhood to adulthood.) o Duchenne: affects only males, appears between the ages of 2 and 6. o Becker :symptoms appear later

Duchenne Muscular Dystrophy is diagnosed from many symptoms in many ways. Since the disorder is most likely going to be inherited, doctors will look at the medical history of the family. Once the background of family history is done, a physical examination of the patient will occur. The examinations are done in various ways. One of the first examinations that physicians do would be the CK ( creatine kinase) level blood test. Creatine Kinase is an enzyme that disclosures out damaging muscles

Duchenne Muscular Dystrophy (DMD) is a lethal genetic X-linked disease results from the mutation in the reading frame of the dystrophin protein, and it affects mostly boys in their muscle and cardiopulmonary function. Although there are no effective treatments to cure DMD patients right now, scientists consistently explore more methods to come up with the practical treatments. One of the most popular and valid approaches is a gene-editing therapeutic method – CRISPR/Cas9 Genome Editing. It adapts

Duchenne Muscular Dystrophy Imagine how it would be like if you can’t run and have to be in a wheelchair at a young age. You would face lot’s of difficulties like having to get up and walking. A rare disease called Duchenne Muscular Dystrophy can do this to you. Duchenne is a disease with rapidly worsening muscle weakness. It is not very well know. Boys are more likely to have it them girls because boys don’t inherit a flawed dystrophin gene. This gene protects you from Duchenne. This rare disease

Duchenne Muscular Dystrophy, referred to as DMD, is the most severe form of all muscular dysrophies. It is rapidly progressive and occurs primary in boys. DMD is caused by a recessive mutation in the X chromosome. It can be inherited by either parent however, it can also be present with no family members having the mutation. DMD is caused by a lack of dystrophin. Dystrophin is a protein found in muscles that enables the muscle tissues to repair themselves. Symptoms can appear in infancy

Abstract Muscular Dystrophy (MD) is a group of genetic diseases in which the voluntary muscles are affected. MD causes weakness and degeneration of muscles progressively overtime. It is most common in young males; but in rare cases it can occur in females. MD is caused by mutations on the X-chromosome gene that prevents the body from producing an essential muscle protein called dystrophy, in which without it muscles weaken (Leung & Wagner, 2013). There are 9 major types of MD, which include Becker