Tourette Syndrome is characterized by several indicators including muscular tics‚ vocal or phonic tics‚ disinhibited thoughts‚ emotional differences including difficulties in emotional regulation‚ obsessive compulsions and rituals. The characteristics and frequency of indicators can change throughout a “Touretter’s” life time. The onset of Tourette Syndrome is usually in childhood between the ages of 5 and 10 (average 7) years old. People with Tourette Syndrome have little or no control over the
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Burn-Out The desease of the modern workforce Introduction Role-Play Theory Bore-Out Burn-Out Tips and Tricks Bore-Out History For years‚ it was always just about the burnout - the excessive demands. Now it has been recognized that even under load‚ called bore out‚ can make you sick. The bore out syndrome is primarily a phenomenon of the service economy. A craftsman can not pretend that he would work. In professions where you have to deliver results bore out hardly occurs. In administrations
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Angelman syndrome is a genetic disorder that cause developmental delay and neurological problems. There is sometimes sleep disturbances‚ seizures‚ jerky movements‚ frequent laughter or smiling and usually always happy. The people that have this tend to not use many words‚ or none at all. Most likely they are very hyper and have little balance. An older term that people use to use would be‚ happy puppet syndrome‚ but it is no longer an accepted term. When people have Angelman syndrome‚ they appear
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Asperger syndrome is an autism spectrum disorder and is considered a high functioning form of Autism. Autism spectrum disorders are also known as pervasive developmental disorders and can affect social skills and communication. Asperger syndrome can also delay the development of motor skills and cause sensory problems. While there is no cure for Asperger syndrome‚ there are treatments to help teach the skills affected by Asperger to patients to help them cope with the disorder. Research is currently
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1 Do you think that education of children with Down syndrome is really important? 2 Do you think there is any specific process for educating this kind of children? . 3 As a doctor‚ do you think having an educational website will be useful and will affect these children’s life? 4 In your opinion what could be the most important aspect in designing this website for children with Down syndrome? 5 Do you think by designing a suitable website according to their disabilities these children will
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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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Down Syndrome Report by: SCHOOL SUX The chromosomal abnormality involved in most cases of Down syndrome is trisomy-21‚ or the presence of three copies of the 21st chromosome. As a result‚ the affected person has 47 chromosomes in all body cells instead of the normal 46‚ although how this causes the condition’s symptoms is not yet known. Scientists assume that the reason for the abnormal chromosomal assortment is the fertilization of an ovum having 24 chromosomes by a sperm with a normal assortment
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How Genetics Influence Down Syndrome Julia Henry PSY 104 Professor Vincent July 7‚ 2013 How Genetics Influence Down Syndrome Genetics play such an vital role in our development. Every individual carries genes from their mother and their father. Characteristics such as height‚ eye color‚ if we have curly or straight hair are all determined through the our genes and specifically our chromosomes. Many times‚ parents inadvertently pass genes on to their children through their DNA that may contribute
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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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Angelman syndrome (AS) is an infrequent genetic condition that has a considerable impact on a person’s nervous system which causes them to have severe physical and intellectual disabilities; I will briefly define these in the commentary (Genetic Disorders‚ 2015). Harry Angelman identified the condition in three children in 1965 however in today’s research it is found in one in sixteen million people.(Angelmanuk.2015).Therefore the reason the research has been so motivational is due to it being very
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