Cultural-Bound Syndrome Yasenta Newman Immaculata University July 31‚ 2012 Dr. Sudol-Regan PSY 608 The term culture-bound syndrome was included in the fourth version of the Diagnostic and Statistical Manual of Mental Disorders. The term cultural-bound syndrome is said to be recurrent with specific patterns of abnormal behavior that can be linked to a particular DSM-IV-TR diagnostic category. Many of these patterns is said to be considered illnesses. The particular symptoms‚ development
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Turner Syndrome Intro Turner Syndrome is a genetic disorder involving a chromosomal defect in females. Turner Syndrome occurs when a woman is missing part or all of an X-chromosome. Though this disease has a wide range of side effects‚ the most common are physical characteristics such as short height and incomplete development. It all depends on how many of the body’s cells are affected by the changes to the X chromosome. This disease affects one in every 2‚500 - 3‚000 girls‚ with 800 affected
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Intro Fetal alcohol spectrum disorders is a term that is used to describe a range of problems that can occur to a fetus if the mother consumes any amount of alcohol during her pregnancy. Fetal alcohol syndrome is the most severe form of fetal alcohol spectrum disorders and has the most visibly identifiable characteristics. Alcohol drastically interferes with the growth and development of several body systems such and the brain and spinal cord‚ facial features and even causes many mental‚ behavioural
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Down Syndrome‚ or DS‚ occurs when a trisomy is found in the twenty-first chromosome leaving three genetically identical chromatids. Down Syndrome is often seen as a disability that limits people while society is also portraying it as a defining characteristic that makes these unique people societal outcasts. Down Syndrome is taken very lightly instead of receiving the attention and care that it requires. In order to understand Down Syndrome‚ one must know the outcome and impact of Down Syndrome‚ one
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Todd’s syndrome‚ more frequently referred to as Alice in Wonderland syndrome‚ it is a disorienting neurological condition that primarily targets children‚ mostly young woman between ages of 2-13. Alice in wonderland syndrome affects human visual perception and involves an array of symptoms that include transient altered perception of the shapes of inanimate and animate objects that appear to be smaller or larger than normal. There can also be an impaired sense of passage of time or the feeling of
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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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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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Paul Keel CDV 106 Cassandra Johnson December 2‚ 2013 Script for Fragile X Presentation Slide 1. FRAGILE X SYNDROME Slide 2. Fragile X syndrome (FXS) is a genetic disorder and the leading cause of inherited mental retardation. Children with this syndrome often have significant delays in learning‚ autistic-like behavior‚ hyperactivity‚ and a distinctive physical appearance Slide 3. The term “fragile X” comes from the finding that the X chromosomes of affected individuals have a
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