Cited: Board‚ A.D.A.M. Editorial. Compartment Syndrome. U.S. National Library of Medicine‚ 18 Nov. 0000. Web. 09 Oct. 2012. . [->0] - http://en.wikipedia.org/wiki/Compartment_(anatomy)
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A Case Study on Compartment Syndrome of the Forearm in a soccer player Objective: To describe the evaluation‚ diagnosis‚ and current treatment of a men’s soccer player with compartment syndrome of the forearm. Background: The forearm is the most common site for compartment syndrome in the upper extremity. The compartments of the forearm include the volar (anterior or flexor)‚ and the dorsal (posterior or exterior). Both bone forearm fractures and distal radius fractures are common initial
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The disease I chose was compartment syndrome because it’s very rare‚ fewer than 20‚000 US cases per year. Compartment syndrome is when a very dangerous and very painful condition cause from pressure builds up from internal bleeding or swelling of the tissues‚ the pressure decreases blood flow‚ depriving muscles and nerves of needed nourishment. The cause of this disease is often causes by injury‚ such as a fracture‚ that causes bleeding in a muscle which then causes increased pressure in the muscle
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Exceptionality Report: Angelman Syndrome The Exceptional Child Andrea Gamber-Smith Dr. Harry Angelman discovered the disease that came to share his name‚ Angelman Syndrome in 1965. Angelman syndrome is impossible to diagnose until approximately the age of three to seven when symptoms become evident. The features of Angelman’s syndrome include a stiff body‚ little or no speech‚ constant giggling or laughter‚ and an easily excitable personality. There are
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Diarmuid Sugrue Angelman Syndrome SYMPTOMS Angelman Syndrome is a neuro-genetic disorder involving the chromosomal region 15q‚ between positions 11-13. The symptoms primarily include intellectual development retardation‚ epilepsy‚ speech impairment‚ ataxia‚ and persistent laughing or smiling. CAUSATIVE MUTATIONS A healthy individual receives 2 copies of the 15 chromosome‚ one maternal and one paternal. The chromosomal region 15q11-13 (base pairs 23‚133‚488-23‚235‚220)‚ contains the gene
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Hunter Syndrome Hunter syndrome is a rare genetic disease that almost always occurs in males. This incurable disease is also called mucopolysaccharidosis II (MPS II). This disorder is caused by the deficiency of the lysosomal enzyme iduronate-2-sulfatase (I2S). This enzyme is needed to successfully break down glycosaminoglycans‚ as part of the body’s normal recycling and renewal process. In a person with Hunter syndrome‚ enzyme I2S is missing or not working correctly. It is the accumulation
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s Rett’s Syndrome Website: http://understandingrettsyndrome.webs.com History Rett Syndrome is a developmental disorder experienced almost always in girls‚ and is first recognized during infancy. Before the discovery of this disorder‚ incidents of Rett Syndrome were mistaken for many other neurologic disorders such as Autism‚ Cerebral Palsy‚ or Nonspecific Developmental Delay‚ especially in females. An Austrian physician‚ Dr. Andreas Rett‚ first described this
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Down Syndrome Down syndrome is a genetic condition that typically causes some level of learning disability and a characteristic range of physical features. Most babies born with Down’s syndrome are diagnosed with the condition after birth and are likely to have: reduced muscle tone leading to floppine eyes that slant upwards and outwards a below average weight and length at birth Although children with Down’s syndrome share some common physical characteristics‚ they do not all look the same
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Marfan Syndrome Have you ever wondered about the diseases that you can get from your parents? One of these major diseases that can change someone’s life is called the Marfan Syndrome. Marfan Syndrome is a disorder of connective tissue that is inherited from the parents. The bones and circulatory system are usually the parts of the body that are longer and the ones that are changed because of the disease. There are many things that can cause a disease. Marfan syndrome is caused by a mutation
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Down Syndrome What is Down Syndrome? Where does it come from? Is there a cure? About one in every 800 American babies is born with Down syndrome‚ and it is estimated that about 350‚000 people in the United States‚ and just under 6 million people worldwide live with this condition today. There is a false impression that pregnancy screening has eliminated or substantially reduced the incidence of Down syndrome in the population. Despite years of screening‚ the Down syndrome population in the
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