What Are Some Signs of Asperger’s Syndrome? When he was eight years old‚ your son Ben was identified as having Asperger’s Problem‚ a high performing function of Autism. My wife and I realized that when Ben was just three‚ four and five years of age he turned quickly frustrated because he didn’t know how to use words to convey what he needed. For example‚ he’d uphold a door he could not open and protest and cry until someone discovered what he needed. We started to say the phrase he needed to state
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the room‚ I saw a female with moon facies and truncal obesity. Instantly‚ Cushing’s syndrome came to my mind. However‚ when I spoke to her I found her speech to be largely incomprehensible‚ she was obviously mentally delayed and had abnormal dentition. My nephrology professor entered the room only to tell me that this patient is suffering from a very rare genetic disorder called Laurence-Moon/Bardet-Biedl syndrome. He asked me to
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Williams-Beuren Syndrome: Controversies in the Complex Behavioral and Cognitive Profile of a Unique Genetic Disorder Zachary Blaker November 12‚ 2015 (3‚982 words) Introduction Williams-Beuren Syndrome (WBS) is a rare neurodevelopmental disorder typically characterized by distinctive facial features‚ cognitive delays accompanied by comparatively strong language and verbal skills‚ deficits in visuospatial construction‚ and hyper-social personality traits (Martens et al. 2008)
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The Black Quarterback Syndrome is based on the biases people have towards the first person known as pioneers‚ that take on a role uncommon to the cultural norm. Even if the person has the qualification to obtain the role. Many cultural shift are currently taking place as the equality of life is expanding but resistance exist as mention by Davis‚ due to the indifference‚ their “distant brought on by gender‚ age‚ race‚ economic class‚ and education that others may just not experience with others
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blocking the majority of these receptors‚ especially the extrapyramidal syndrome (EPS) which is most bothersome to both patients and doctors putting often an end to treatment. This inconvenience is explained by the following fact: their antagonizing activity is not directed to the mesolimbic receptors specifically‚ and ends up acting on all D2 receptors in the brain causing side effects. When they block D2R in the striatal pathway‚ we have extrapyramidal symptoms resembling those of Parkinson’s disease
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Acquired Immunodeficiency Syndrome (AIDS) Acquired Immunodeficiency Syndrome (AIDS)‚ human viral disease that ravages the immune system‚ undermining the body’s ability to defend itself from infection and disease. Caused by the human immunodeficiency virus (HIV)‚ AIDS leaves an infected person vulnerable to opportunistic infections—infection by microbes that take advantage of a weakened immune system. Such infections are usually harmless in healthy people but can prove life-threatening to people
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Hypertrichosis: The Werewolf Syndrome The disease Hypertrichosis‚ also known as “The Werewolf Syndrome‚” causes unwanted/abnormal hair growth either in one spot or all over an affected person’s body. There are two main types: Naevoid‚ and Congenital. Naevoid Hypertrichosis‚ is where the hair grows in one spot on the body‚ sometimes the limbs but usually proportional in the facial area. Congenital is where hair covers a majority of the body‚ sometimes right after birth! In severe cases‚ the
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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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Lesch Nyhan Syndrome Lesch Nyhan Syndrome (LNS) was first reported in 1964 by Michael Lesch and William L. Nyhan. It is a rare disorder located on the x chromosome. It is a sex-linked trait‚ which means that it is passed from mother to son. This condition can be inherited or occur spontaneously as a result of a genetic mutation. It usually appears once in every 100‚000 male births. Since the defective gene is recessive‚ females almost never exhibit symptoms of the disease. However‚ they can be
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argue that this ever busy lifestyle is from always being connected (through cell phones‚ text messaging‚ voicemail‚ email‚ etc.) and never making the separation from work and play. That is why a growing disease in today’s culture is Chronic Fatigue Syndrome (CFS)‚ at about half a million people in America alone. Currently‚ the exact cause is unknown because there is no lab test‚ scan‚ or blood test that diagnoses CFS. It was once believed that this disease was closely linked with Epstein-Barr
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