Tracie Emmerich Professor Debbie Seale Biology 101 TR‚ 8:30-11:30 am 3/6/2012 Triple X Syndrome Triple X Syndrome is a sex chromosome abnormality in which there are three X chromosomes instead of the usual two found in most females. Triple X Syndrome is also known as Trisomy X‚ Triplo X Syndrome‚ and XXX Syndrome. The first published report of a woman with a karyotype with a 47‚ XXX was by Patricia A. Jacobs in 1959 at a hospital in Scotland. Most people have 46 chromosomes‚ occurring in
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Diabetes‚ Metabolic Syndrome and Obesity: Targets and Therapy Open Access Full Text Article Dovepress Review open access to scientific and medical research The economic impact of obesity in the United States This article was published in the following Dove Press journal: Diabetes‚ Metabolic Syndrome and Obesity: Targets and Therapy 17 August 2010 Number of times this article has been viewed Ross A Hammond Ruth Levine economic Studies Program‚ Brookings institution‚ washington DC‚
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Williams Syndrome‚ also known as Williams-Beuren disorder is a congenital genetic disorder characterized by a deletion in parts of chromosome 7. It is “a multisystem disorder‚ caused by deletion of the Williams-Beuren syndrome chromosome region‚ spanning 1.5 to 1.8 million base pairs and containing 26 to 28 genes.” (Pober‚ 2010‚ p 239) Demographics Williams Syndrome affects 1 in 10‚000 children throughout the world and an estimated 20‚000 to 30‚000 in the United States. (Williams Syndrome Association
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Andres Schmidt Biology Period- I 05/21/13 Coffin-Lowry Syndrome (CLS) Coffin-Lowy Syndrome Definition: Coffin–Lowry syndrome is a genetic disorder that is X-linked dominant and which causes severe mental problems sometimes associated with abnormalities of growth‚ cardiac abnormalities‚ kyphoscoliosis‚ as well as auditory and visual abnormalities. Grange S. Coffin in 1966 discovered this syndrome‚ in the University of Columbia New York United States of America. Grange S. Coffin Grange
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Pain Syndrome is a term used to describe pain in the front of the knee around the patella. It is a condition in which the cartilage under the patella is damaged due to an injury or a chronic stress. Patellofemoral pain syndrome is also known as runner’s knee‚ jumper’s knee‚ and can also be referred to as‚ anterior knee pain syndrome. Patellofemoral pain syndrome is more commonly found in the female sex‚ and in young adult athletes. However‚ studies have shown that patellofemoral pain syndrome can
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Pshycotic Depression may cause strong delusions‚ depression‚ hallucinations and even social impairement. When a patient suffers from Cotard’s Syndrome Type I they tend to experience multiple delusions. Patients with Cotard’s Syndrome Type II suffer from anxiety‚ delusions‚ hallucinations (auditory) and depression; this is also the most common. Biologically speaking‚ there is no clear problem with the people that suffer from Cotard’s.
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Turner’s Syndrome Turner’s syndrome is a genetic condition in which a female does not have the usual pair of two X chromosomes. This medical disorder affects about 1 in every 2‚500 girls. I do not know exactly what causes Turner syndrome‚ but researchers know that it is the result of a problem with a girl ’s chromosomes either not being there at all or only part of it is still there. I think the most known effects of the condition vary widely with girls with Turner syndrome. It all depends
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Angelman syndrome (AS) is an infrequent genetic condition that has a considerable impact on a person’s nervous system which causes them to have severe physical and intellectual disabilities; I will briefly define these in the commentary (Genetic Disorders‚ 2015). Harry Angelman identified the condition in three children in 1965 however in today’s research it is found in one in sixteen million people.(Angelmanuk.2015).Therefore the reason the research has been so motivational is due to it being very
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Zellweger syndrome is one of a group of four related diseases called peroxisome biogenesis disorders‚ a group of deadly genetic diseases that claim the lives of children usually before they reach their first birthday. This syndrome is the most common type of peroxisome biogenesis disorder. The disease is caused by defects in any one of 13 genes‚ called PEX genes‚ required for the normal formation and function of peroxisomes. Peroxisomes are cell structures that break down toxic substances and synthesize
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White Nose Syndrome (WNS) affects bats causing them to wake up more often during hibernation and use up their stored fat reserves that were supposed to last throughout the winter. The lack of fat reserves forces bats to fly around for the search of food‚ but unfortunately most of the bats tend to starve‚ freeze and die. Data has been collected to provide information about the areas associated with White Nose Syndrome in bats. Results shown White Nose Syndrome in bats does not impact all of North
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