Muscular Dystrophy Essay

Muscular Dystrophy Causes/Risk Factors: Genetics is a key factor in potentially developing a form of muscular dystrophy, as it is caused by a gene that protects muscle fibers suddenly becoming defective. However, this particular genetic mutation can abruptly occur while an embryo is still developing in the egg of the mother. Muscular dystrophy can occur in an individual of any age, sex, or race. The most common form of MD diagnosed, Dechenne, is most often found in males of a youg age. However

Duchenne Muscular Dystrophy Genetic Disorder Introduction to Duchenne Muscular Dystrophy Duchenne muscular dystrophy (DMD) is one of many types of muscular dystrophy disorders, which affect the muscle fibers. It is the most aggressive form of muscular dystrophy. The muscle fibers gradually become weaker and incapacitate the affected individual. “DMD is a recessive, fatal, X-linked disorder occurring at a frequency of about 1 in 3,500 new-born males (NCBI, 2014).” Males are more susceptible to inherit

Muscular Dystrophy in Pediatric Patients A muscular dystrophy is a group of diseases that is associated with progressive weakness and loss of an individual’s muscle mass. The condition causes the abnormal genes to interfere with the production of proteins needed to form healthy muscles. There is no medical cure for muscular dystrophy and related diseases, but strategies such as medication and therapy are used to manage the symptoms and slow the course of the disease. There are more than 30 types

Muscular dystrophy is a genetic disease that causes weakness and loss of muscle mass. Muscular dystrophy is a rare disease. 349 out of 2.37 million males aged between five and twenty-four had Duchenne or Becker muscular dystrophy in 2007. Males are more likely to be affected. It is very rare for females to have the disease. There are different types of muscular dystrophy. One type is called Duchenne muscular dystrophy. Most people that have muscular dystrophy have this type. Another type is called

Case Study: Muscular Dystrophy Scott Shannon PHGY 220- Gerald McGraw October 31, 2014 Muscular dystrophy is a group of inherited diseases in which voluntary muscles or the muscles that control movement, gradually weaken. MD is caused by mutations in genes responsible for proper function and muscle structure. This disease in some forms, can also affect the heart and other organs. The mutations disable the cells from properly maintaining muscle. This advances to muscle weakness

Muscular Dystrophy Muscular dystrophy or MD, a disease that causes progressive weakness in muscles. This occurs when a mutation that alters the production of proteins that the muscles need. MD is more common in boys, and in most cases, symptoms begin in childhood, but could not appear until later in life, depending on the type of MD. As of now, there is no known cure for MD but, there are treatments to slow the progression of the disease. One major sign of MD is muscle weakness. There are many

Muscular Dystrophy and Its Effect on the Body System Muscular Dystrophy also known as MD, is made up of a group of genetic diseases where muscle fibers are unusually susceptible to damage and the damaged muscles become progressively weak. Muscular Dystrophy is caused by certain defects with a specific type of gene known as the abnormal gene. Majority of muscular dystrophies come from an inherited disease referred to as X-linked disorders or genetic diseases in which mothers can transmit to their

1.0 Abstract Duchenne Muscular Dystrophy is a degenerative X-linked recessive disorder usually resulting in death in the late third decade. Mutation of Dystrophin gene at Xp21 disrupts the mRNA reading frame resulting in absent dystrophin protein in muscle cells. Currently no therapy can counteract the disease effectively. Exon skipping with oligonucleotide administration restores the reading frame of the mRNA to produce truncated but functional dystrophin and requires repeated administration

Medical News Today, muscular dystrophy is a disorder that is characterized by the progressive loss of muscle mass and consequent loss of strength(Newman). There are specific causes that effect the body, and thus creates certain symptoms that are noticeable initially, and symptoms that occur later on in the process. I will be discussing the causes, symptoms-both initial and later, diagnosis, treatment, and prognosis. In order for one to be classified as having muscular dystrophy, there are certain

The Genetics of Duchenne Muscular Dystrophy Duchenne muscular dystrophy is the most common genetic disease fatal in children, it is a severe and rapidly progressive muscle disease with symptoms that first become evident due to the affected child showing early motor developmental delay; for example, presentation of Gower’s sign, a diagnostic indicator of proximal muscle weakness characterised by the affected having to “walk” their hands up their body to stand due to little strength being present in