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    Turner Syndrome

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    Turner Syndrome It was first described in 1930‚ and first diagnose in 1959. Now a days‚ 1 of 2‚000 females are born with this syndrome. Turner syndrome (also known as TS) is named after the famous endocrinologist Henry Turner‚ who was the first person to described and published any findings about this syndrome. This condition is also known as Bonnevie-Ullrich syndrome‚ Gonadal dysgenesis‚ and Monosomy X. The syndrome is a non-inherited chromosomal condition that only occurs in females. It’s cause

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    Stockholm Syndrome

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    thoroughly? yes Corrie Nicholas Sedita English 101 November 25‚ 2012 Stockholm syndrome: Cause and Effect Stockholm syndrome; an issue that lends it name from a 1973 robbery of Kreditbanken in Stockholm‚ Sweden‚ in which two robbers held four bank employees hostage from August 23 to 28. These robbers shared a space with their victims and became emotionally attached and even defended them after. Today this syndrome is viewed as a psychological response to a situation where the victim has had their

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    Down Syndrome

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    flenfef Down Syndrome is named after John Langdon Down‚ the first British doctor who first described the condition in 1987. It wasn’t until 1959‚ however‚ that an extra chromosome was identified as the cause. One in every 691 babies in the the United States are born with Down syndrome. Making Down syndrome the most common genetic condition. Approximately 400‚000 Americans have Down syndrome and about 6‚000 babies with Down syndrome are born in the United States each year. Down syndrome (DS)‚ also

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    Down Syndrome

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    Down Syndrome Thesis: When someone sees a child or an adult with Down syndrome they automatically single them out‚ every person in this world is different‚ with a disability or with out‚ but that doesn’t mean they need to be treated differently. I. Causes A. Mental Disorder B. Mothers age C. Not inherited D. Most common E. Amniocentesis II. Symptoms A. Problems at birth B. Size C. Other issues D. Facial features III. Severities A. Ranges B. Trisomy 21 C. Mosaic D. Mosaic

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    Down Syndrome

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    DOWN SYNDROME Down Syndrome is a congenital disorder arising from a chromosome It comes from a defect involving chromosome 21. The condition leads to impairments in both cognitive ability and physical growth that range from mild to moderate developmental disabilities. Through a series of screenings and tests‚ Down syndrome can be detected before and after a baby is born.  The only factor known to affect the probability of having a baby with Down syndrome is maternal age. Less than one in 1‚000

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    Williams Syndrome

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    Williams syndrome also recognized as Williams-Beuren syndrome is a genetic disorder caused by a deletion of more than twenty five genes from chromosome 7. Although Williams syndrome is often non-hereditary‚ the chances of the syndrome being passed on if an individual with Williams syndrome has a child are fifty percent. Individuals born with Williams syndrome often possess distinctive facial features which make the syndrome easily recognized. These features include wide spaces between their teeth

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    Asperger's Syndrome

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    Asperger’s Syndrome Today there are many different types of disabilities and syndromes. When you have a child to be diagnosed with a disability or a syndrome life can suddenly become overwhelming. This is especially true if they have been diagnosed with Asperger’s Syndrome. Parents sometimes feel guilty because their child has a disability or syndrome. Parents may feel that they are responsible for their child’s disability or syndrome. Parents may feel guilty about their child being diagnosed

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    Down Syndrome

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    14 November 2011 Outline INTRODUCTION Thesis Statement: Although Down syndrome is used as a general term‚ several forms of this syndrome exist. I. Diagnosis A. Discovery B. Cause II. Types A. Trisomy 21 B. Translocation C. Mosaicism III. Expectations From Therapy CONCLUSION Down syndrome Lot’s of people fail to realize that several forms of Down syndrome exist. “Down syndrome is a set of mental and physical symptoms that result from having an extra copy

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    Down's Syndrome

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    Down’s Syndrome Down’s syndrome is a genetic condition involving an extra chromosome‚ this change occurs around the time of conception. A person with Down’s syndrome has forty-seven chromosomes instead of the usual forty-six. A relatively common genetic disorder‚ Down’s strikes 1 out of 600 babies. In 95 percent of all cases‚ the disorder originates with the egg‚ not the sperm‚ and the only known risk factor is advanced maternal age-at age 35‚ a woman has 1 chance in 117 of having a baby with

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    Marfan Syndrome

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    is like that. Have you ever heard of something called Marfan syndrome or MFS? It is a genetic disorder that about one in every five thousand people have and there is a fifty percent chance that it can be passed on to the next generation ("What Is Marfan Syndrome?"). Marfan syndrome is an abnormal condition characterized by elongation of the bones‚ and abnormalities in the cardiovascular system and the eyes (Hamilton). Marfan syndrome is a genetic disorder that can be inherited from ancestors and

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