identity; she must address the letters to Mr. John Smith‚ and he will never reply. Jerusha catches a glimpse of the shadow of her benefactor from the back‚ and knows he is a tall long-legged man. Because of this‚ she jokingly calls him Daddy-Long-Legs. She attends a "girls’ college‚" but the name and location are never identified. Men from Princeton University are frequently mentioned as dates‚ so it might be assumed that her college is one of the Seven Sisters. It was certainly on the East Coast
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Tourette Syndrome is a neurological disorder that is characterized by sudden repetitive and involuntary movements or vocalizations that are generally termed “tics”. These tics can have different degrees of intensity ranging from simple to complex. Simple motor tics are brief‚ sudden‚ and repetitive movements that involve a limited number of muscle groups. They include facial grimacing‚ eye blinking and other eye movements‚ and head or shoulder jerking. Simple vocalizations include repetitive sniffing
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Noonan Syndrome Nicole Mitchell Dr. Hendricks Principles of Biology 1114 April 19‚ 2013 Mostly everyone in the world has heard of some type of genetic disorder. But most people haven’t even heard or understand about Noonan Syndrome. Noonan syndrome is a genetic disorder characterized by distinctive facial features‚ developmental delay‚ learning difficulties‚ short stature‚ congenital heart disease‚ renal anomalies‚ and bleeding difficulties. Noonan syndrome affects a good percent of the world
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Klinefelter Syndrome is a syndrome in which a person has an additional X-chromosome. It is not life consuming‚ but rather people who have this syndrome can live perfectly normal lives proper treatment and care‚ if precautions are taken early on. Dr. Harry Klinefelter in 1942 first identified the syndrome. Now some may ask what Klinefelter syndrome is. Klinefelter syndrome is a syndrome in which a person inherits an extra X-chromosome making their genetic makeup xxy instead of the normal How it occurs
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the disease. Progeria Research Foundation also funds medical research that is specifically aimed at finding the cause. Treatments and cures for this syndrome are more reasons that the foundation funds research for the disease (How PRF was formed). Progeria is an outcome of a fault in the Lamin A(LMNA) gene (Hutchinson-Gilford Progeria Syndrome 2012). The LMNA gene has codes that are for two proteins‚ Lamin A and Lamin C. These proteins play a big role in stabilizing the inner membrane of
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Running head: METABOLIC SYNDROME Metabolic Syndrome James Doucette College of Western Idaho Abstract Metabolic syndrome is an emerging diagnosis in the medical field that has effects on patient care. Becoming familiar with it and having it become a common part of patient care will‚ if used appropriately will increase the lives of those who have become affected with or are at risk of becoming diagnosed with metabolic syndrome. Metabolic syndrome is a constellation of risks
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Hunter Syndrome Hunter syndrome is a rare genetic disease that almost always occurs in males. This incurable disease is also called mucopolysaccharidosis II (MPS II). This disorder is caused by the deficiency of the lysosomal enzyme iduronate-2-sulfatase (I2S). This enzyme is needed to successfully break down glycosaminoglycans‚ as part of the body’s normal recycling and renewal process. In a person with Hunter syndrome‚ enzyme I2S is missing or not working correctly. It is the accumulation
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Kallmann ’s Syndrome ABSTRACT Kallmann’s syndrome is a rare disorder which affects predominantly man. Typical characteristics are a failure to go through puberty and an absent sense of smell. Although the disease is not life threatening‚ somebody with kallmann’s syndrome has an hormonal imbalance hypogonadotropic hypogonadism due to GnRH deficiency because a small area of his or her brain called the hypothalamus is unable to work properly. Specialised hormone replacement therapy is available
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Marfan Syndrome Wesley Thompson Jim Hutchins Biomedical Core 1110 November 19‚ 2011 Marfan syndrome is a variable‚ autosomal-dominant disorder in the connective tissue with distinct physical characteristics. The principal features affect the cardiovascular system‚ eyes and skeleton. This condition affects the connective protein that forms the structural support for tissues outside the cell. This disease is a result of a faulty makeup of chromosomes. Since MFS (Marfan Syndrome) is an
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Ophelia Syndrome Study Skills November 12‚ 2012 In the essays of Diagnosing and Treating Ophelia Syndrome and Everybody is Ignorant on Different Subjects two topics are discussed which are related‚ in that they both have to do with learning and being able to think as an individual. The Ophelia Syndrome is not processing the ability to create one’s own opinion. Ophelia is a character in the play Hamlet. She is described as a helpless child and has a “Lord” or authoritative figure that forces
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