captors. Although not deeply documented a form of the syndrome may have afflicted slaves after being freed under the Emancipation Proclamation. The master presided over the land the slaves were allotted to‚ no outside contact may be made‚ escape often had penalty of death‚ and all facilities were provided by the master. Some slaves were against the idea of leaving slavery‚ thereby entranced by the syndrome. ( Krasnec) Stockholm syndrome is a term used to describe when a kidnap or barricade victim
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Marfan’s Syndrome Marfan syndrome is an inherited connective-tissue disorder transmitted as an autosomal dominant trait. It is distributed worldwide‚ has a high prevalence rate and has pleiotropic manifestations‚ meaning one gene influences multiple traits that do not seem to be related. Mutations of the FBN1 gene on the 15th chromosome (more specifically chromosome 15q21.1) cause Marfan syndrome. The FBN1 gene is coded to make a glycoprotein called fibrillin-1
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Down Syndrome (DS) is the most common chromosomal condition in the United States‚ affecting about 1 in every 700 babies (CDC). This condition is also known as Trisomy 21‚ due to there being an extra copy of chromosome 21 (CDC). This extra chromosome results in changes in the development of the brain and body‚ which in turn can lead to cognitive and physical challenges (CDC). Some hallmark physical characteristics include almond shaped eyes that slant up‚ smaller hands and feet‚ shorter stature‚
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Zellweger syndrome is one of a group of four related diseases called peroxisome biogenesis disorders‚ a group of deadly genetic diseases that claim the lives of children usually before they reach their first birthday. This syndrome is the most common type of peroxisome biogenesis disorder. The disease is caused by defects in any one of 13 genes‚ called PEX genes‚ required for the normal formation and function of peroxisomes. Peroxisomes are cell structures that break down toxic substances and synthesize
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Introduction To the Disorder Asperger’s syndrome (AS)‚ originally described by Hans Asperger in 1944 (Attwood‚ 2007‚ p. 23)‚ was historically considered a distinct high-functioning subtype of autism. It is now considered simply an autism spectrum disorder (ASD) following a change to the Diagnostic and Statistical Manual of Mental Disorders (DSM) in 2013 (Kite‚ Gullifer‚ & Tyson‚ 2013). “Autism spectrum disorders are severe disorders of development that can affect social interaction‚ communication
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Thoracic Outlet Syndrome is a complex disorder characterized by a constellation of signs and symptoms resulting from a compression of blood vessels and nerves in the thoracic outlet region where they exit the chest. The thoracic outlet is a space located between the thorax (rib cage) and the clavicle (collarbone) which contains major blood vessels and nerves. The thoracic outlet is the area through which nerves and blood vessels travel to and from the arm. Thoracic Outlet syndrome is considered
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Prader Willi Syndrome Prader Willi syndrome‚ or more commonly known as PWS is a disorder that causes “obesity‚ intellectual disability‚ and shortness in height” (Mayo Clinic). PWS is a not a common disorder. According to MNT‚ it is estimated that “one in 25‚000 people have PWS in the US and it affects an estimated 350‚000 to 400‚000 people worldwide.” However‚ PWS is the most common genetic cause of life-threatening childhood obesity that has been identified to date in genetic clinics. There is
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Medical factors that may impact the behavior: Bonnie has been diagnosed with Prader-Willi syndrome a life-threatening disorder which begins in childhood. Individuals with Prader-Willi syndrome develop an insatiable appetite which results in chronic overeating and obesity (United States National Library of Medicine‚ 2015). Bonnie’s diagnosis of Prader-Willi syndrome is a strong causal link for strong desire to obtain food. Bonnie also has multiple disabilities and sensory problems. Individuals with
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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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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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