...“prayer to the earth for [her] sister on her graduation (Pinskoski 98)”. She tries to prompt her sister through this piece, who is suffering from the Down’s syndrome. This poem is definitely inspirational for her sister all the individuals suffering from Down’s syndrome but also to all readers who are unfortunate in any way. This poem is enriched with creative metaphor, powerful word choice other various elements. Nonetheless, this poem is basically comparing the one extra chromosome that causes Down’s syndrome and one extra leaf of four leaf clover. Mary Pinkoski’s poem is a great poem, compares the four leaf clover and Down’s syndrome. Firstly, the name of the poem “Four Leaf Clover”...
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...REC 408- Research | A Study of Early Fine Motor Intervention in Down’s Syndrome Children | Dr. Hutchinson | 3/24/2011 | Aparicio, T.S. and Balaña, J.M. (2007). A Study of Early Fine Motor Intervention in Down’s Syndrome Children. Early Child Development and Care, 179(5), 631–636. Introduction This study researches the marked delay in acquisition of fine motor skills in Trisomic-21/Down’s Syndrome children are undeniable. The study begins with an affirmation that the cause of this deficit could be found in a different environment for which early intervention is essential. Purpose of Study The purpose of this study was to analyze fine motor interventions in Down’s syndrome children. Tables were drawn to record the behavioral objective tested, the help needed and the result obtained. The child’s progress was measured through initial examination and periodic re-examinations. Methods * Participants - A sample of 30 children (18 boys and 12 girls) with primary Trisomy in pair 21 * Procedures - Two subgroups were formed according to their initial ages - Social interview was held with the parents. * Measures - Diagnostic examination and an observation period Results The effect on the fine motor DQ (FmDQ) was established by means of a prior diagnostic examination and regular check-up for which the Brunet-Lèzine Scale was used. In each ANOVA, the FmDQs attained in each check-up were compared with those subjects who had...
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...unborn baby has Down's syndrome By DAILY MAIL REPORTER UPDATED: 12:13 GMT, 7 March 2011 Doctors have developed a blood test to check unborn babies for Down’s syndrome. The approach could save pregnant women from having the invasive examinations currently available, which raise the risk of miscarriage. Current blood tests can only tell if a baby is at risk of Down's Syndrome. Scientists from Cyprus, Greece and Britain said the new technique correctly identified 14 Down syndrome cases and 26 normal foetuses in a blind test. They believe it will also be possible to diagnose the condition earlier on. Study author Philippos Patsalis, of the Cyprus Institute of Neurology and Genetics, said: 'The method is simple and fast and easy to perform in every genetic diagnostic lab worldwide because it does not require expensive equipment, software or special infrastructure. 'The test is the first worldwide to demonstrate 100 per cent sensitivity and 100 per cent specificity in all normal and Down's syndrome pregnancies examined.' Down's syndrome is a genetic disorder that causes physical and learning disabilities and raises the risk of heart disease. Infants with the condition have three copies of the Chromosome 21 instead of the normal two. It affects about one in every 700 live births but women of 40 are 16 times more likely to have a Down's child than a 25-year-old. At present all pregnant women are offered screening to see if their baby is at risk of Down's syndrome. For a firm...
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...Genetics Down Syndrome Down syndrome (DS) or Trisomy 21 is a complex developmental genetic disorder in which a person has 47 chromosomes instead of 46. Normally, a fertilized egg has 23 pairs of chromosomes. But in most cases, people living with Down syndrome have an extra copy of chromosome 21 also known as Trisomy 21, which is responsible for 95% Down syndrome cases and most common genetic cause of human mental retardation, with an incidence of 1-600/1-1000 live births. It is also responsible for premature pregnancy failure. It is the leading cause of cognitive impairment. Down syndrome occurs because of an abnormality characterized by an extra copy of genetic material on all or part of the 21st chromosome. Every cell in the body contains genes that are grouped along chromosomes in the cell's nucleus or center. There are normally 46 chromosomes in each cell, 23 inherited from your mother and 23 from your father. When some or all of a person's cells have an extra full or partial copy of chromosome 21, the result is Down syndrome. Down syndrome is associated with mild to moderate learning disabilities, developmental delays, characteristic facial features, and low muscle tone in early infancy. Many individuals with Down syndrome also have heart defects, leukemia, early-onset Alzheimer's disease, gastro-intestinal problems, and other health issues. The symptoms of Down syndrome range from mild to severe. Life expectancy for individuals with Down syndrome has dramatically...
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...Title of the News Story: Dubai girl with Down’s syndrome beats all odds Date: 6 July 2014 Author: Dhanusha Gokulan Source (name of the newspaper): Khaleej Times newspaper http://www.khaleejtimes.com/kt-article-display-1.asp?xfile=data/nationgeneral/2014/July/nationgeneral_July20.xml§ion=nationgeneral Introduction: The article in the Khaleej Time’s newspaper I have chosen is talking about the highly successful story of a 20 year old Indian photographer a Dubai resident named Aarti Shah. What makes her more special is the fact that she a girl that has Down’s syndrome and is able to do much more activities and hobbies as for both regular people and people who are diagnosed with Down’s syndrome. In the article they mention her life story, where she has studied and what are her inspirations and the jobs that she occupies right now. Article Summary: The article celebrates the achievements of the talented Aarti Ajay Shah. Although she has Down’s syndrome, Ajay still beats all the odds and makes everything seem possible to all. Ajay Shah is the youngest between her brothers and sisters and has lived in Kenya before 12 years ago, where she had went to a regular school and been in a regular school environment. After living in Kenya her family moved to Dubai and for the last 5 years she has been a student in Al Noor Training Center for children with special needs, the center is located in the Barsha area in Dubai. Aartai’s mother has told the Khaleej times...
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...THE REPORT DOWN SYNDROME ( TRISOMY 21 ) Down syndrome is a developmental disorder caused by an extra copy of chromosome 21 (which is why the disorder is also called "trisomy 21"). Having an extra copy of this chromosome means that each gene may be producing more protein product than normal. Cells seem to tolerate this better than having not enough protein, or having altered protein due to a mutation in the DNA sequence. However, producing too much protein can also have serious consequences, as seen in Down syndrome. Genes on chromosome 21 that specifically contribute to the various symptoms of Down syndrome are now being identified. Down syndrome is typically caused by what is called nondisjunction. If a pair of number 21 chromosomes fails to separate during the formation of an egg (or sperm), this is referred to as nondisjunction. When that egg unites with a normal sperm to form an embryo, that embryo ends up with three copies of chromosome 21 instead of the normal two. The extra chromosome is then copied in every cell of the baby's body. Interestingly, nondisjunction events seem to occur more frequently in older women. This may explain why the risk of having a baby with Down syndrome is greater among mothers age 35 and older. In rare cases Down syndrome is caused by a Robertsonian translocation, which occurs when the long arm of chromosome 21 breaks off and attaches to another chromosome at the centromere. The carrier of such a translocation will...
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...Development and Child Growth ECE 205 Introduction to Child Development April 9, 2012 We talk about the descriptions of child development and growth stages and what they mean and how we look at those stages and how a child will develop and growth through these changes as well. When we talk about growth we are talking about the actual size and the physical changes that a child makes over time, We talk about how the cells in the body change and with time change and expand or enlarge which is what increases the growth and the height of a child, also their weight, the circumference of their head, hands, shoe size, arm growth, and last but not least there body shape as well. Allen, K & Martoz, L (2010) When we look at children they all develop differently some will growth mentally at a faster pace than others, and others will grow physically faster than others. Infants will become more of their surroundings and with those stages of infant growths and starting out would be the rooting and sucking reflex which is a very big part of growth because that is a part of survival and that also starts to create them to be able to turn their heads. Some of the other major growths that happen with infants when they are starting to grow would be the Moro reflex, Palamar grasp reflex, babinski reflex, and last but not least the stepping and walking reflex. As those stages start to happen then you have the cognitive development and those stages would start out by the senorimotor stage...
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...Trisomy: Humans have 23 pair of chromosomes or in total 46 chromosomes. 22 pairs are autosomes and 1 pair is sex chromosome. The autosomes carry information regarding the whole body except for sex of that human. The sex is determined with the sex chromosome. If the sex chromosome contains two XX then the sex is said to be female, and if it is XY it is male. A trisomy is a chromosomal abnormality in which the total number of chromosomes exceeds, and the person has 47 chromosomes instead of 46. There are three major types of trisomy, depending upon the addition of chromosomes. These are Patau Syndrome, Edward Syndrome and Down’s syndrome. Children born with trisomy have multiple birth defects, which include poor intellect and delayed milestone....
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...Cri du chat, also known as “Cat’s Cry” syndrome or 5p- (5 p minus) syndrome occurs when there is a deletion in chromosome 5 (Genetics Home Reference). According to the Genetics Home Reference website, most cases of Cri du Chat are not inherited. The deletion occurs randomly during production of reproductive cells or in early development. People with Cri du Chat most often have no familial history of the disease. Only about ten percent of the cases of Cri du Chat are inherited from unaffected parents. Most of the time in this situation, the parent’s chromosome is rearranged. The material is not gained or lost, but is located on different parts of the chromosome. So, when the material is moved to create gametes or chromosomes in a developing...
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...Prader-Willi Syndrome is a genetic disorder that affects chromosome number fifteen. Some of the common signs of this syndrome are obesity, eyes with narrower shape, small hands, feet and stature. Often the muscle tone is decreased and as a consequence motor development is delayed. Individuals affected usually have mild learning disabilities and only a small portion have average or above average IQs. Their long term memory is stronger and efficient than their short term memory. Most students with Prader-Willi Syndrome have difficulty working with numbers and calculations. They usually perform better when working with reading, writing, drawing, and when working with technology. Behavior issues are directly associated with the syndrome as well...
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...Cat eye syndrome is a genetic condition , a way to describe it is to say that it is an abnormality in chromosome 22. It can lead to a coloboma of the iris witch is how it got its name . The eyes look cat-like but work the same as a normal human . Cat eye syndrome or “Schmid Fraccaro syndrome” is a rare condition caused by the short arm and a small section of the long arm of human chromosome 22 being present three (trisomic) or four times (tetrasomic) instead of the usual two times. The name “cat eye syndrome” is derived from a distinctive eye (ocular) abnormality that is present in a little over half affected individuals. Most cases of eye cat syndrome are not hereditary , the condition generally occurs even during the formation of...
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...The Physical Health of Older People with Learning Disabilities: The Nurse’s Role Student Professor Course Date Introduction In the UK, the term “learning disability” is used to depict people who have an impairment of intellectual ability that strongly affects their daily activities. For that reason, they need constant supervision, help and care from authorized nursing personnel, in order to lead a rather normal life. Other countries use terms such as “intellectual disability” or “mental retardation”. (Perry, Hammond and Marston, 2010) According to Doctor Nicola Davies (2008), older patients that suffer from learning disabilities have greater physical healthcare need than other patients, however due to a lack of proper training of the nursing personnel or a misunderstanding of their requirements, their needs are most often neglected. People who suffer from learning disabilities are often faced with an inability to learn new skills or understand complex information, and with an impairing of their social function. This affects their development both physically and psychologically. (Davies, 2008) Lindsey (2002) states that people with learning disabilities have a lower understanding of a healthy lifestyle and have a reduced ability to detect illness. Usually, when people with learning disabilities feel ill, they do not draw the attention of others about their condition. For this reason, it is important for nurses to be highly aware for changes in the behavior of...
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...leaves not much time for learning because the toileting, hygiene, and eating do take a big part of the day. The teachers usually have a full time assistant in the classroom or two depending on the need in the classroom; this helps the Special Education teacher complete tasks in the classroom. The teacher can work on a student one on one and the assistant can help with the other students needs. (Severe Intellectual Disabilities and Multiple Diablites, 2007) Some of the intellectual disabilities that teachers may encounter I have found are ADHD (Attention Deficit hyperactivity Disorder), Angel man syndrome, Aspersers Syndrome, Autism, Cri Du Char, Down Syndrome, Dysphasia, Dyspraxia, Epilepsy, Fragile X, Klinefelter Syndrome, Pervasive Developmental Disorder, Prader-willi Syndrome, Rett Syndrome, Trismoy, Soto’s Syndrome, Tourette Syndrome, Tuberous Sclerosis, and Williams Syndrome. (Activ, 2001) References Activ (2001) Types of Intellectual Disabilities. Retrieved on July 13, 2001 from http://www.activ.asn.au/3/3017/8/types_of_intellectual_disability.pm Severe Intellectual Disabilities and Multiple Disabilities. Pat Mimms. Retrieved from Special Education for Today’s Teachers: An Introduction, by Michael S. Rosenberg, D avid L. Westling, and James M cLeskey....
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...Edward's Syndrome Edward's Syndrome, also known as Trisomy 18 Syndrome, was discovered in 1960 by Dr. John Edward. It is a very rare inherited genetic disorder that is likely in one out of every five thousand births. Children with the syndrome have an extra chromosome 18, causing the child to have many malformations and mental retardation. Nineteen out of twenty of the children with the Edward's Syndrome die before their first birthday. There are three types of the Trisomy 18 Syndrome. The first one is most common it's called Full Trisomy 18. In this case a full extra chromosome is present in each cell. This type is not hereditary. The second type is very rare, it's called Partial Trisomy 18. This type of the syndrome can be hereditary. It occurs when only part of the extra chromosome is present in each cell. The third type is Mosaic Trisomy 18 this is also very rare. The extra part if the chromosome is only present in some of the cells, not all. The defects of Edward's Syndrome can target the brain, heart, craniofacial structures, kidneys and stomach. The children that make it thorough birth appear fragile and weak, many are underweight and have micrognathia. Many of the surviving children have these problems because of the malformed extra chromosome, just one little chromosome can really make or break someone's life. The syndrome can be diagnosis by taking a blood sample from the fetus to look at the chromosome line up. Edward's Syndrome can also be diagnosed by a few other test...
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...What is Down syndrome? Down syndrome is genetic disorder that causes lifelong mental retardation, developmental delays and other problems. Down syndrome varies in severity, so development problems range from moderate to serious. Down syndrome is the most common genetic cause of severe learning disabilities in children, occurring in one in every 700 to 800 infants. Increased understanding of Down syndrome and early interventions make a big difference in the lives of both children and adults with Down syndrome. Down syndrome is also known as Trisomy 21 syndrome. Trisomy 21 is due to an extra copy of chromosomes number 21. Instead of having the normal two copies chromosomes number 21, the person with Down syndrome has three copies of chromosomes 21. Meaning normally a fertilized egg has 23 pairs of chromosomes. In most people with Down syndrome, there is an extra copy of chromosome 21. (Rogers, 2007, pg.6) The formal story began in 1866, when a physician named John Langdon Down published an essay in England in which he described a set of children with common features who were distinct from other children with mental retardation. Down was superintendent of an asylum for children with mental retardation in Surrey, England when he made the first distinction between children who were cretins (later to be found to have hypothyroidism) and what he referred to as "Mongoloids." Down based this unfortunate name on his notion that these children looked like people from Mongolia,...
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