"Down syndrome case study" Essays and Research Papers

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    child with autism‚ learning disability & Mental retardation which includes Down syndrome. Children with Down syndrome have the following difficulties: below average cognitive ability‚ poor in working memory‚ difficulty in producing clear speech and socially sensitive. These problems should be addressed in choosing the right approach for them. As a Future Sped Teacher‚ we aid in giving the children with Down syndrome their best chances in leading independent and functional life. It is because

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    examined the practical application of the Selye’s general adaptation syndrome basing on my own experience. Recently‚ I have faced a stressful situation when I needed to change my place of living. It might be a lucky moment‚ but it is still a disturbance of my everyday routine. Additionally‚ I was afraid of the fact that it would take some time before I could get settled in my new place. According to the Selye’s general adaptation syndrome‚ the first phase is called “alarm” which represents a generic somatic

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    # 258844 FELIPE DIAZ DOI: 6/15/2008. The patient is a 63-year-old male rotary slot operator who sustained injury to his wrists due to repetitive motion of flipping corrugated sheets. The patient was subsequently diagnosed with carpal tunnel syndrome‚ unspecified upper limb. As per medical report dated 1/18/16‚ patient complains pain in his right elbow and bilateral hands and wrists. He has increased pain in bilateral upper extremities from elbow to hands worse on the right. He states uses Transcutaneous

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    PATHOLOGY CASE REPORT XL dominant Alport Syndrome: a rare condition and a rare mode of genetic transmission INTRODUCTION Alport syndrome (AS) is a rare abnormality of glomerular basement membrane caused by mutations in several different genes‚ all of which encode particular forms of type IV collagen‚ a major component of basement membrane. It is characterized by chronic renal failure leading to end-stage renal disease (ESRD) and is often associated with sensorineural deafness (Kanski 2003)

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    XYY Syndrome‚ Jacob Syndrome XYY Syndrome‚ better known as the Jacob Syndrome is a rare genetic disorder which affects males due to an extra Y chromosome. Healthy males have 46 chromosomes including one X and one Y chromosome. Men with XYY syndrome have 47 chromosomes‚ two of which are Y chromosomes. It is not known why the extra Y chromosome occurs. The disorder is present at birth and is estimated to occur in one out of every one thousand live births (1). In very rare instances‚ the syndrome

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    3.3. Slowing Down The Error Propagation Speed In this section‚ we will explain the studies that made for slowing down the error propagation. In this project‚ we will attack this research problem from multiple angles. First‚ we will consider different algorithms and gauge whether such choices have a significant impact on error propagation profiles. Second‚ we will consider compiler optimizations that slow error propagation. 3.3.1 Impact of the algorithms Error propagation behavior is connected with

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    Identifying the barriers and facilitators to participation in physical activity for children with Down syndrome. Images Authors: Barr M; Shields N Author Address: School of Physiotherapy and the Musculoskeletal Research Centre‚ La Trobe University‚ Melbourne‚ Vic.‚ Australia. Source: Journal Of Intellectual Disability Research: JIDR [J Intellect Disabil Res] 2011 Nov; Vol. 55 (11)‚ pp. 1020-33. Date of Electronic Publication: 2011 May 10. Publication Type: Journal Article Language:

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    Article summary: Cognitive skills‚ behavior and learning potential of preschool children with Down Syndrome. University of Jaen (pronounced Ha-en)‚ Spain. This article describes the testing of the cognitive ability and learning potential of preschool children who have Down Syndrome. The children were compared against another group of children of the same age who do not have Down Syndrome. The testing occurred within the constructs of Vygotsky’s Social Learning theory. Both groups of children

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    There are several cases of which a young woman has suffered from Turner syndrome and needed a way to help gain the height differences. One article by Toft and Rehan (2014) has opened the idea too using growth hormones to offset those height differences. The way the drug works is that it is released from the pituitary gland into the liver where it releases a insulin-like growth factor which tells the muscles‚ bones‚ and ligaments to grow (Toft and Rehan‚ 2014). In-fact there are ways that the growth

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    others are passed down through family like traits. The latter are called genetic diseases‚ since inheritance plays a role in procuring the disease. There are countless of studies concerning genetic diseases. Gene mapping is used in describing how a gene could have been mutated or altered in a way for a condition to be developed. Knowing the loci for diseases also helps in finding a treatment. Many diseases can attest to certain genes being involved in their development. Duane syndrome is one example

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