Muscular dystrophy

genetic diseases that are classified as muscular dystrophies. Muscular dystrophy is the weakness and degeneration of the skeletal muscles that often control movement. In muscular dystrophy, abnormal genes, also called mutations, interfere with the production of the proteins that are needed to form healthy muscle in the body. There are many kinds of muscular dystrophies and symptoms are more than likely begin during childhood. With different kinds of muscular dystrophy, comes many different symptoms and the disease is different for everyone that has it. Symptoms of muscle dystrophy vary with the different types of the disease. The symptoms of each type appear at different ages and can also be in different…

Burgen, M., Stam, H., & Pangailia, R. F. (2015, July 10). Prevalence of Fatigue, Pain, and Affective Disorders in Adults With Duchenne Muscular Dystrophy and Their Associations With Quality of Life. In Archives of Physical Medicine and Rehabilitation. Retrieved October 6, 2016. In this article, Michael Burgen, Henk Stam, and Robert Pangailia explain how muscular dystrophy is a genetic, recessive, neuromuscular disease in which there is a lack of protein dystrophin which helps stabilize…

Every year, thousands of people, mostly young 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…

Muscular Dystrophy is a disease which leads to muscle weakness and loss of strength. This disease begins at an early age and symptoms appear during the early stages of childhood and it progressively destroys and deteriorates the muscles. Among the many types of Muscular Dystrophy, the most common and severe form is Duchenne Muscular Dystrophy (DMD). Duchenne Muscular Dystrophy is an inherited disorder and unlike other forms of Muscular Dystrophy, it is the one that develops and worsens quickly…

Muscular dystrophy is a type of hereditary disorder that can cause muscle weakness and can ultimately lead to the decay of skeletal muscles. A diagnosis of this disease can create a reduced quality of life and the inability to perform basic day-to-day function. Since this disease is genetic and is caused by a mutation, it is more likely for an individual to be diagnosed if a previous member of the family has had it before. The most common type of muscular dystrophy is known as Duchenne Muscualr…

Duchenne Muscular Dystrophy In this world, there are many diseases that are being caused by the X chromosomes or the Y chromosomes. Some of the diseases could be passed down from generation onto the next because it is gene and some of the diseases can be treated and which later on causes for it to make it worse. The diseases that would always be there would be Down Syndrome, Huntington’s Disease, Hemophobia, and many more. As you can see, this paper is going to be able a genetic disease that is…

160116 Duchenne Muscular Dystrophy “Muscular dystrophy (MD) is a genetic disease characterized by progressive weakness and degeneration of the skeletal or voluntary muscles which control movement” (Muscular dystrophy, 2013). Muscular dystrophy is classified into nine major types that each affect specific muscle groups, certain age groups and are identified by different signals. Duchenne muscular dystrophy most commonly affects males and is targeted at younger children (Facts about Muscular…

specific types of Muscular Dystrophy only affect men. For instance the Duchenne is most commonly known for affecting young children, but Duchenne muscular dystrophy is also know to only affect makes. This type of condition and reductions the muscle in mass and causes it to diminish and become weaker and weaker. This disorder is know to have significant affects on young boy, and by the age of 12 they will require the use of a wheel hair. With time the limbs and spin will become considerably…

Muscular dystrophy is genetic disorder that is caused by a mutation in the genes, causing muscle mass to become weaker and degenerated. This is a consequence on the genes with mutation that have a missing protein responsible for muscle health. There are over forty types of muscular dystrophy and each varies in characteristics and severity. Duchenne muscular dystrophy is the most common type and only boys are affected by it. Characteristics can vary depending on the type of muscular dystrophy,…

Muscular dystrophy is a group of noncommunicable diseases that is passed down through heredity lines. Noncommunicable diseases are diseases that developed in humans without other species interference and that cannot be passed between people. Muscular dystrophy can be broken up into nine major forms: Myotonic, Duchenne, Becker, Limb-girdle, Facioscapulohumeral, congenital, Oculopharyngeal, Distal, and Emery-Dreifuss. Muscular dystrophy can appear at any time in one’s life, typically in infancy or…