Reye Syndrome Reye Syndrome is an extremely rare‚ non-contagious disease thought to be triggered by aspirin use. The actual origin of the disease is unknown. Reye’s Syndrome‚ occasionally called Reye-Jacobsen’s Syndrome‚ is known to follow any viral infection. Two of the most common viral infections it precedes is influenza‚ "the flu"‚ and chicken pox. A now-familiar warning on bottles of aspirin‚ most notably Tylenol‚ is not to give Tylenol to a child who is recovering from the chicken
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Turner Syndrome Turner syndrome affects 3% of all females prior to birth‚ with only around 1% of these ‘in utero’ cases surviving to term; it is not inherited from either parent‚ but purely a ‘chance’ mutation. Despite this‚ it has become the most common genetically determined abnormality amongst females‚ and can have detrimental effects on systemic wellbeing throughout life. Turner Syndrome is a sex-linked genetic disorder which only affects females‚ and can present symptoms in several organ
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Victoria Haskins Biology Honors Mr. Kelly March 6th‚ 2017 Edwards Syndrome Edwards syndrome‚ also known as Trisomy 18‚ is a condition caused by a mistake in meiotic cell division resulting in an extra chromosome 18 in a developing baby (Source 1). This condition disrupts normal development‚ potentially fatally‚ even before birth (Source 1). Major characteristics of the disorder include a delay in growth‚ a low birth weight‚ and other major medical complications (Source 1‚ Source 3). Professor of
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Savant Syndrome 1. How does Savant Syndrome help us understand the nature of intelligence? Savant Syndrome is an exceedingly rare phenomenon in which people with disabilities have remarkable abilities and talents. The uniqueness of this disease has enabled us to better understand the nature of intelligence and cognition. Savant syndrome helps us to better comprehend the specialization of the left and right hemispheres in our brain. Because savants are especially talented in areas such as numbers
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involved in their development. Duane syndrome is one example of these genetic diseases. People who suffer from this rare condition have the limited
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Münchausen Syndrome and Münchausen Syndrome By Proxy Münchausen Syndrome There are many syndromes in people’s lives. All of the sydromes have been effecting people’s health negatively in people lives since the existence of human being. One of the most interesting syndrome is Munchausen Syndrome. It is related to unreal illness. In other words‚ Some people who has münchausen syndrome can cause an illness own their own. Therefore‚ they are actually clever and have medical information. Due to their
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There are several cases of which a young woman has suffered from Turner syndrome and needed a way to help gain the height differences. One article by Toft and Rehan (2014) has opened the idea too using growth hormones to offset those height differences. The way the drug works is that it is released from the pituitary gland into the liver where it releases a insulin-like growth factor which tells the muscles‚ bones‚ and ligaments to grow (Toft and Rehan‚ 2014). In-fact there are ways that the growth
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WAGR Syndrome WAGR (Wilms’ tumor‚ Aniridia‚ Genitourinary abnormalities‚ and mental Retardation) Syndrome is a contiguous gene deletion syndrome that is caused by a deletion in chromosome 11. The acronym for the syndrome comes from the various symptoms that are caused by the deletion – wilms’ tumor‚ aniridia‚ genitourinary abnormalities‚ and mental retardation. Wilms’ tumor is a tumor that is found in the kidneys that causes nephroblastoma‚ cancer of the kidneys. Aniridia‚ the absence of the iris
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Kartagener’s syndrome is an autosomal recessive disorder affecting the cilia within the body. Autosomal recessive means that one or more of both the parents’ genes responsible for encoding the cilia’s structure are mutated. This essay will focus on the etiology‚ clinical manifestations and anatomic alterations while also exploring diagnostic and treatment modalities. Cilia are the tiny hair-like structures found in many organ systems including the respiratory and reproductive systems. It was diagnosed
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Bloom’s Syndrome is a rare genetic disease known for affecting someone’s physical and genetic traits‚ this disorder can cause problems for whoever is diagnosed with it. Bloom’s Syndrome is a disease characterized by how its identified‚ its frequency‚ how it was discovered‚ its symptoms‚ and its treatments. Bloom’s Syndrome is identified as an autosomal disorder. An autosomal disorder is when the defected gene is carried on a chromosome other than one of the sex chromosomes. Bloom’s Syndrome happens
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