Mental Illness Research Questions - Munchausen Syndrome What illness are you researching? Factitious Disorders Munchausen Syndrome Ganser Syndrome What is the definition of your disorder? What might be physical/noticeable characteristics of this disorder? Munchausen syndrome is a mental disorder where a person repeatedly pretends to have severe illnesses‚ when they actually are the ones causing the illness to themselves. Those who have this illness will mostly complain of physical pain‚ as opposed
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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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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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happened‚ I glared down at a surging pain that vibrated through my whole body‚ mainly sourcing from my left ankle. My ankle was completely turned backwards. I frantically yelled out to my instructor‚ “MY ANKLE IS BROKEN!” As he sprinted over to the other side of the gymnasium where I was laying in agony‚ I could see an audience starting to gather. He informed me that the ambulance was on its way and that my mother had been notified. Five
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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 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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METABOLIC SYNDROME LEARNING OBJECTIVES At the end of lecture students should know – Definition of Metabolic Syndrome – Visceral obesity is an indicator of the syndrome and an independent marker for CVD – Current and some potential future treatment options. METABOLIC SYNDROME CONCEPT (Not New) • 1923 - Kylin first to describe the clustering of hypertension‚ hyperglycemia‚ hyperuricemia • 1936 - Himsworth first reported Insulin insensitivity in diabetics • 1965 - Yalow and Berson
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According to the national heart‚lung‚and blood institute‚ in 2003‚ approximately 40‚000 infants and 150‚000 adults were reported with RDS meaning about one person out of 6‚800 has RDS. It is very important to be careful with this syndrome because if an infant or breathing machine tried to apply some pressure to the lungs there is a high chance of it to rupture causing air to leak making the lung collapse sinking in even farther which turns it into a more severe case‚ usually this
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Case Discussion Beal’s syndrome (OMIM # 121050) is a disorder of connective tissues. The syndrome was first explained by Beal’s and Hecht in 1971. It is inherited as an autosomal dominant disorder that is characterized by multiple flexion contractures‚ arachnodactyly‚ severe kyphoscoliosis‚ abnormal pinnae and muscular hypoplasia. It is caused by a genetic mutation in FBN2 gene (encoding the extracellular matrix micro fibril fibrillin 2) on chromosome 5q23. The FBN2 gene provides instructions for
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Angelman Syndrome By Ciera Carr Dr. Glimps 2006 Carr 1 Ciera Carr Dr. Glimps Research Paper Angelman Syndrome Angelman syndrome is a genetic disorder that is caused by a couple of different attributes. The first one is “a deletion on chromosome 15 of maternal origin or paternal uniparental disomy”(Curfs‚ 2004‚ p. 1263). There has also been found that some people with the disorder have no deletion on the chromosome at all. Angelman syndrome was first discovered in 1965 by a doctor
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