Muscular Dystrophy Essay

muscular dystrophy has many forms and therefore symptoms can vary between the variations. Overall symptoms include the weakening of skeletal muscles and the defect and death muscle tissues. Duchenne muscular dystrophy is the most common and affects young boys such as Eddie. Eddie is an 11 year old boy and has been diagnosed with Duchenne muscular dystrophy. The symptoms appeared at the age of 5 and had led to the weakening of his leg and arm muscles and the eventual need of a wheelchair. Some of

Muscular Dystrophy: Roots, Cause, and Current Research Muscular dystrophy is an inherited disease that was discovered in 1861, by Guillaume B.A. Duchenne. Muscular dystrophy is a group of heredity disorders characterized by rapidly-worsening muscle weakness. The trait for muscular dystrophy may be transmitted as an autosomal dominant which means a disorder that has two copies of an abnormal gene that must be present in order for the disease or trait to develop. In this case, if some original

Muscular dystrophy (MD) is a group of genetically transmitted diseases characterized by progressive symmetric wasting of skeletal muscles without evidence of neurologic involvement (Lewis, 2011). There are four different types of muscular dystrophy. The four types are Duchenne, Becker, Landouzy-Dejerine, and Erb. Duchenne muscular dystrophy is the most common type among children. It only affects boys; it’s passed down from the mother. Duchenne muscular dystrophy is created from X-linked recessive

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 commonly begins in the

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

Muscular dystrophy (MD) is the progressive weakening and deterioration of the skeletal muscles controlling movement. There isn’t only one type of this disease; MD is a group of over 30 genetic diseases. The diseases differ in many ways. Age of onset may be seen in infancy and childhood, or develop during teenage years through later in life. Types of MD differ in muscle distribution and extent of weakness, and rate of progression. Duchenne MD, as in James’ case, is the most common form. It’s primarily

Duchenne muscular dystrophy was first discovered by Guillaume Benjamin Amand Duchenne in the 1860’s, but due to lack of medical knowledge little was known until the 1980’s. It was in 1986 that researchers that were supported by the MDA, muscular dystrophy association, identified the particular X-chromosome that leads to DMD, Duchenne muscular dystrophy. Dystrophin is the protein that is associated with the gene and was named in 1987.The DMD gene is the second largest gene to date, and it produces

word muscular dystrophy? Some people may have no idea as others may have firsthand experience dealing with this disease or having extensive knowledge on the subject. The purpose of this paper is to inform any healthcare professional, anyone taking care of someone with muscular dystrophy, or anyone interesting on being informed about Muscular dystrophy. This paper will provide an overview of muscular dystrophy as well as the different types and the problems associated with muscular dystrophy. Also

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