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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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 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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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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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 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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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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Chromosomal Disorders 1. Name the condition. Edwards Syndrome (or Trisomy 18) 2. Outline the chromosomal abnormality. Trisomy 18‚ or Edwards syndrome‚ occurs when a person has a third copy of material from chromosome 18 instead of the usual two copies. 3. What chromosomes are involved? Chromosome 18 is the only chromosome involved with this disorder. 4. What does it affect? The majority of children born with Edward ’s syndrome appear both fragile and weak; many are underweight. Their
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Aarskog Syndrome Description Aarskog syndrome (also known as Aarskog–Scott syndrome‚ faciodigitogenital syndrome‚ shawl scrotum syndrome and faciogenital dysplasia) is a rare autosomal X-linked inherited disorder that affects a person’s height‚ muscles‚ skeleton‚ genitals‚ and appearance of the face. It mostly affects at birth and the symptoms usually become apparent by the age of 3years. Unfortunately‚ Aarskog syndrome is a lifelong condition without a cure. Some people with Aarskog syndrome are born
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Edwards Syndrome‚ also known as Trisomy 18‚ is a genetic syndrome of severe to profound mental retardation. It is caused by the presence of an extra chromosome 18 in some or all of the cells in the body. Babies with this condition typically do not survive but for a few months after birth. About sixty percent of newborns with this condition die within the first week‚ and eighty percent do not survive through the first month
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