"Down syndrome thesis" Essays and Research Papers

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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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    Down's Syndrome

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    Victoria Downs Mr. Eddie Paden English 101 April 3‚ 2014 Her name is Haley; she is healthy‚ smart‚ and excels in school. Haley is one of my younger sisters‚ and she has Down’s syndrome. I was young when my parents found out that they were going to have a child with Down’s syndrome‚ and we weren’t sure how things would be for our family or for Haley. As I grew up I came to realize what the next lifetime with her as a sister would entail. Today Down’s syndrome is a common disorder in the United

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    Down Syndrom

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    Abstract a) Down syndrome b) Interesting topic c) Understanding why down syndrome occurs Introduction a) Who discovered Down syndrome b) What is Down syndrome Body research A. What Causes it and is it inherited? 1-Trisomy 21 2-Mosaic Down syndrome 3-Translocation Down syndrome B. How Down syndrome affects Kids 1-Physical features 2-Learning C. Risk factors 1-Advancing maternal age 2- Being carriers of the genetic translocation for Down syndrome 3-Having

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    Down's Syndrome

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    Down’s Syndrome Abstract This research is aimed at getting theoretical and practical knowledge about Down’s Syndrome. Psychological aids such as observation‚ Informal Interviews and case histories were used to gather information for this project. The conclusion drawn was that it is possible for individuals suffering from Down’s Syndrome to lead a fairly normal and highly satisfying life if they are provided with a loving and nurturing environment at home. Introduction The aim of this paper

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    Noonan Syndrome

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    Noonan Syndrome Noonan syndrome is a genetic disorder that was once known as Turner-like syndrome. It is a mutation of several genes where they develop proteins that are continuously active; which ends up disrupting the control of the cells growth and division resulting in abnormal developments of the body. Noonan syndrome can affect a person’s physical appearance in multiple ways‚ along with their mental state of mind. This syndrome equally affects males and females. Noonan syndrome was first

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    Angelman Syndrome.

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    Angelman Syndrome In America‚ about 6 million students are known to have some kind of intellectual disability. Intellectual disabilities are not always determined by the IQ level of an individual but rather how they react to their peers‚ self-perception‚ problem solving‚ personal care‚ etc.. It could develop before birth‚ after birth or even in one’s later life. Usually‚ these disabilities are caused by mutation in one of the chromosomes of a fetus. For example‚ some syndromes are the result of

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    Skills of Children with Down Syndrome (DS)” Author : Leila A. Ricci (California State University-Los Angeles) Journal : Article appeared on International Journal of Special Education (On-line version)‚ Vol. 26 No. 3 2011 Before the late 1960’s‚ the scientific community was dearth with researches on reading for children with Down syndrome and until the 1990’s‚ the exception was the child/children with Down syndrome (DS) who could read (Oelwein

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    Coffin-Lowry Syndrome

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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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    Turner Syndrome Papers

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    Turner Syndrome is a genetic disorder that effects development in women‚ per TurnerSyndrome.Org. Women who have Turner Syndrome have one X Chromosome instead of two full X Chromosomes that most females are born with. One of the X chromosomes are “dropped” during Meiosis‚ when the sex cells divide to form eggs in females. It is not usually inherited. Turner Syndrome can affect the development of several body systems in those who have them. Turner Syndrome is believed to be a random error during the

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    Turner Syndrome Essay

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    Chromosomal Disorder: (Turner Syndrome) Introduction Turner Syndrome is a condition that only alters the development of girls and women. Most girls and women have two full and complete X chromosomes while girls with turner syndrome have only part of the second X chromosome. Women and girls are diagnosed with turner syndrome have features such as slow growth rates‚ a webbed neck‚ broad shoulders‚ and widely spaced nipples. They also have swelling hands and feet‚ heart defects‚ kidney problems‚ and

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