"Burnout syndrome" Essays and Research Papers

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    Nail Patella Syndrome

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    1. Explain what must happen in order for Greg and Susan to have a child with O type blood and nail-patella syndrome. Greg needs to pass down his chromosome 9 which carry the alleles‚ n and i. Susan also has the n and I alleles on chromosome 9. If both these alleles from both parents are passed down‚ it will create the allele Nnii which produced the blood type O and nail patella syndrome. 2.  Determine all possible parental and recombinant gametes produced by Greg and Susan. Greg’s parental

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    Klippel-Fiel Syndrome

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    Klippel–Feil syndrome is a very rare disease. It was reported for the first time in 1912 by Maurice Klippel and André Feil. It has been characterized by the fusion of any 2 of the 7 cervical vertebrae. The syndrome occurs in a heterogeneous group of patients unified only by the presence of a defect in the formation or segmentation of the spine. Klippel–Feil syndrome can be identified by shortness of the neck. Those with the syndrome have a very low hairline and the ability of the neck to move is

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    Marfan Syndrome Essay

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    Marfan syndrome is a multisystem disorder resulting with clinical manifestations typically involving the skeletal‚ ocular‚ and cardiovascular systems. Skeletal abnormalities of Marfan syndrome include disproportionate overgrowth of the long bones‚ anterior chest deformity due to overgrowth of the ribs‚ and overgrowth of the fingers. A reduced upper-segment to lower-segment ratio to arm span to height ratio of greater than 1.05 due to the overgrowth of the arms and leg is also a major criterion for

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    Shaking Baby Syndrome

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    April 30‚ 2005 Micro. Comp. Shaken Baby Syndrome Imagine yourself as a sweet‚ innocent‚ precious little baby. You are totally dependent upon adults to give you what you need and most importantly love. Your only means of communication is crying so you cry when you need to be fed‚ when you need your diaper changed‚ when you aren’t feeling so well‚ or when you just want some attention. You are crying and someone comes over to you. They pick you up‚ but instead of holding you and comforting

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    Overview Diabetic hyperosmolar syndrome is serious complication that is sometimes experienced by diabetic patients‚ most commonly those with type 2 diabetes. It occurs when the body consistently produces dangerously high blood sugar levels. As a result‚ the body attempts to flush out the excess blood sugar through increased urination. If it is not treated‚ it can become life threatening or even fatal. While the condition often develops in response to an infection or illness‚ it can also be caused

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    Budd Chiari Syndrome

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    advantages and disadvantages? Budd Chiari Syndrome •Clinical term used to describe the manifestation of hepatic venous outflow obstruction •Secondary to hepatic vein thrombosis •Or to the narrowing/occlusion of the inferior vena cava (Khan 2009‚Val DC 2003) Ostial stenosis web thrombus Abdominal vein Liver Stomach Gallbladder Enlarged caudate lobe Inferior vena cava Portal vein (Menon et al.‚ 2004) Budd Chiari Syndrome • Primary type -Endoluminal venous (I.e. Thrombosis

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    Student: Eibhlín Ní Mhuircheartaigh ID Number: 59210388 Qualification: M.Sc. Guidance & Counselling Module: ES551: Wellbeing‚ Society and Lifelong Learning Title of Essay/Seminar Paper: Case Study: School struggles of those living with Asperger Syndrome Please indicate the term and academic year this module was studied: Spring 2010 Term: Autumn  Spring Summer Academic Year: 2009/2010 Is this a re-submission? Yes  No Word length: 2‚735 Date of

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    Foreign Accent Syndrome

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    How foreign is Foreign Accent Syndrome? Christina Stone ENG101 Mr. Link Tuesday October 30‚ 2012 Foreign Accent Syndrome is a rare medical disorder in which a patient develops what sounds like a foreign accent. Further investigation reveals a significant increase in the number of cases over the past few years. This essay will consider some of the reasons why Foreign Accent Syndrome also known as FAS has had such a rapid escalation. The question of whether FAS is

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    The common cause of congenital myasthenic syndromes is genetics‚ affecting the junction where the nerve triggers muscle activity. The inherited autosomal recessive gene exists in both parents‚ who pass the mutated gene to the offspring. The syndrome appears shortly after birth or early childhood. Severity ranges from minor to increasing concentrations of muscle weakness. There are over twenty different genes known to cause congenital myasthenic syndromes‚ as different as each individual. Sometimes

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    Down Syndrome Sociology

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    Evidence suggests that a very significant proportion of children with Down syndrome could be placed successfully in a mainstream school. Research data‚ although still somewhat limited‚[1] indicates that such placements lead to academic as well as social gains and increase the chances of the child making local friendships that extend beyond the school day. These facts have lead increasing numbers of parents to seek an inclusive placement for their child. In some parts of the country[2] over 80% of

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