"Münchausen syndrome by proxy" Essays and Research Papers

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    Mean World Syndrome Essay

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    that television has become the main source for storytelling in society. It is responsible for‚ shaping‚ or cultivating‚ viewers perceptions of social reality. The "Mean World Syndrome"‚ is a term coined by Gerbner (1986)‚ which developed through his innovative research project‚ "the Cultivation theory". The Mean world Syndrome‚ is a phenomenon whereby‚ violent-related content of mass media makes viewers believe that‚ the world is more dangerous than it actually is. This therefore‚ makes the human

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    Cornelia de Lange Syndrome typically presents with a constellation of distinctive features affecting several different parts of the body. There is a wide degree of variation between individuals with the disorder in the presentation and severity of symptoms; however‚ the features described below represent a typical presentation (Deardorff‚ Clark‚ & Krantz‚ 2011). Slow growth during both fetal and post-natal development is a characteristic feature of the disorder. Approximately 90% or more of

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    PTSD syndrome is a serious psychological problem that usually occurs as a result of a traumatic experience and causes fear and a total sense of powerlessness with the patient. Posttraumatic stress disorder (PTSD) with adequate access and above all understanding of this condition can be successful‚ mitigate and eventually completely eliminated. In what way can alleviate the problems and how to overcome the traumatic experiences in the right way‚ find out below . PTSD SYNDROME DEFINITION AND CAUSES

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    Research Paper 2: Angelman Syndrome     Angelman Syndrome (AS) also known as Happy Puppet Syndrome was originally founded in 1965 by an English physician named Dr. Harry Angelman. (NORD 1) According to the Genetics Home Reference‚ “AS is a complex genetic disorder that primarily affects the nervous system”.While exact numbers are unknown due to the fact that some cases are misdiagnosed as cerebral palsy or Autism‚ it is believed that about 1 in 15‚000 people have AS‚ ( Genetics Home Reference 2)

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    Running Head: AMYGDALA & HYPERSOCIABILITY The Role of the Amygdala and Abnormal Social Behavior in Williams Syndrome Abstract Williams syndrome (WS) is a genetic neurodevelopmental disorder often paired with unique behavioral abnormalities like hypersociability‚ reduced fear and a tendency to approach strangers. The amygdala is an integral component of the neural network and has been implicated in social phenotype particularly in emotion and fear. Functional

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    Jacob’s Syndrome Jacob’s Syndrome is a rare chromosomal genetic syndrome where the male has an extra Y male chromosome and ends up having 47 chromosomes with XYY instead of normal 46‚XY (male) or 46‚ XX (female.) It is very rare and happens in only about 1 out of 1‚000 men. The exact reason for this is unknown. In a very rare cases it was passed from father to son‚ but in most cases it is not hereditary. It was first discovered by Patricia Jacobs in 1965. She proposed the suggestion that the

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    Imagine growing old before having the chance to grow up. Hutchinson-Gilford Syndrome‚ commonly referred to as progeria‚ is a disease that has this effect on a significant amount of children around the world. Although there are many different forms of progeria‚ Hutchinson-Gilford Progeria Syndrome is the classic type. The name progeria comes from Greek origin and means “prematurely old”. Those who suffer from this disease take on the effects of early aging. Although their bodies begin to age early

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    Capgras Syndrome‚ a condition that has a tendency to be neglected from the attention of the public. Yet‚ still manages to affect the lives of thousands of people everyday. Media representations of Psychological disorders have a representation to misguide the masses. However‚ a story written by Richard Powers is able to paint an accurate picture as to how this syndrome may affect an individual‚ their lives‚ and the life of the people around them. This novel being “The Echo Maker”(2006)‚ following

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    Hypermobility syndrome is a condition that features joints that easily move beyond the normal range expected for a particular joint. Hypermobility is also known as “double-jointness”. This particular disorder has an unknown discovery date and founder. The causes of hypermobility are family history: disorder is inherited‚ bone structure‚ muscle structure and sense of proprioception which is knowing how far you are able to stretch. Genes that are responsible for the production of collagen are suspected

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    Sudden Infant Death Syndrome Sudden Infant Death Syndrome (SIDS) is defined as “an unspecified medical entity: the sudden and unexpected death of a reasonably healthy child‚ whose passing away remains uncertain following the performance of an adequate assessment of medical history‚ autopsy‚ and death scene examination”(Valdes-Dapena‚1979). SIDS is one of the predominately-unsolved problems of infancy. The number of infants who die each year of SIDS is greater than the number of children who die

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