Peter Pan syndrome‚ is exactly how it sounds. It ’s a disorder that is derived from the novel Peter Pan written by J.M. Barrie that defines those who appear as an adult but their actions are quite childlike. The ‘Peter Pans’ of present society “see the adult world as very problematic and glorify adolescence‚ which is why they want to stay in that state of privilege”‚ according to Humbelina Robles Ortega‚ professor of the Department of Personality‚ Evaluation and Psychological Treatment of the University
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Alagille Syndrome The first documentation of Alagille Syndrome was by a pediatric doctor named Daniel Alagille‚ in France of 1969. Later in 1973‚ Doctor Watson and Doctor Miller noted that the same disease also runs dominantly within a family‚ suggesting that it might be an inherited condition. By 1975 the specific symptoms and conditions were laid out and thus named Alagille Syndrome‚ also referred to as Alagille-Watson or Watson-Miller syndrome. The primary characteristic of Alagille Syndrome is
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Artificial Heart/ Heart Transplants A natural heart has two pumps‚ each has two chambers. The right atrium pumps oxygen-depleted blood from the body into the right ventricle. The right ventricle pumps blood to the lungs. The left atrium sends aerated blood from the lungs into the left ventricle‚ which pumps blood out of the body. With each heartbeat‚ the two atria contracts together‚ followed by the large ventricles. Congestive heart failure is when the heart fails to pump blood. Heart failure
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Metabolic syndrome consists of multiple interrelated risk factors which directly promote the development of atherosclerotic cardiovascular disease (ASCVD).The risk factors include atherogenic dyslipidemia‚elevated plasma glucose‚elevated blood pressure‚proinflammatory and prothromboticstate(1). Prevalence of metabolic syndrome in world population was estimated to be around 20-25%.patients with metabolic syndrome are twice likely to die from Cerebrovascular accident and myocardial infarction.patients
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Kristen Coleman What is Post- Polio Syndrome? Post-polio syndrome (PPS) is an illness that causes symptoms to reappear in individuals who had recovered from polio decades earlier. After recovering from polio‚ some survivors find themselves afflicted again‚ facing a serious condition called post-polio syndrome. PPS is a condition in the nervous system that affects muscles and nerves. What are the symptoms of Post-Polio Syndrome? Symptoms of post-polio tend to show up in a patient gradually
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Treacher Collins Syndrome is believed to be caused by a change in the gene on chromosome 5‚ which affects facial development. About 40 percent of the time‚ one parent has the Treacher Collins Syndrome gene. Geneticists can now determine whether the Treacher Collins gene is a new mutation or one that has been passed on. There are new studies being done to see about the possibilities of there being other genes that could be involved with this syndrome. Treacher Collins Syndrome is believed to be
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1. Explain what must happen in order for Greg and Susan to have a child with O type blood and nail-patella syndrome. Greg needs to pass down his chromosome 9 which carry the alleles‚ n and i. Susan also has the n and I alleles on chromosome 9. If both these alleles from both parents are passed down‚ it will create the allele Nnii which produced the blood type O and nail patella syndrome. 2. Determine all possible parental and recombinant gametes produced by Greg and Susan. Greg’s parental
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Polycystic Ovarian Syndrome The most common female endocrine disorder is Polycystic Ovarian Syndrome (PCOS). As reported by the Polycystic Ovarian Syndrome Association‚ PCOS is the imbalance of hormones in a women’s body which can lead to menstrual cycle changes‚ cysts in the ovaries‚ trouble getting pregnant‚ and other health changes (What is PCOS‚ 2009). The cause of this endocrine disorder is unknown‚ however‚ according to the National Institute of Health (NIH)‚ it is connected to changes in
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Diabetes‚ Metabolic Syndrome and Obesity: Targets and Therapy Open Access Full Text Article Dovepress Review open access to scientific and medical research The economic impact of obesity in the United States This article was published in the following Dove Press journal: Diabetes‚ Metabolic Syndrome and Obesity: Targets and Therapy 17 August 2010 Number of times this article has been viewed Ross A Hammond Ruth Levine economic Studies Program‚ Brookings institution‚ washington DC‚
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Diarmuid Sugrue Angelman Syndrome SYMPTOMS Angelman Syndrome is a neuro-genetic disorder involving the chromosomal region 15q‚ between positions 11-13. The symptoms primarily include intellectual development retardation‚ epilepsy‚ speech impairment‚ ataxia‚ and persistent laughing or smiling. CAUSATIVE MUTATIONS A healthy individual receives 2 copies of the 15 chromosome‚ one maternal and one paternal. The chromosomal region 15q11-13 (base pairs 23‚133‚488-23‚235‚220)‚ contains the gene
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