Noonan Syndrome Noonan syndrome is a genetic disorder that was once known as Turner-like syndrome. It is a mutation of several genes where they develop proteins that are continuously active; which ends up disrupting the control of the cells growth and division resulting in abnormal developments of the body. Noonan syndrome can affect a person’s physical appearance in multiple ways‚ along with their mental state of mind. This syndrome equally affects males and females. Noonan syndrome was first
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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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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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Korsakoff’s Syndrome Korsakoff’s syndrome is a disorder in which a lack of thiamine results in anterograde and retrograde amnesia — those with the disorder exhibit the loss of newly formed memories‚ and a degeneration in their ability to remember events from their past (Spiegel‚ Lim‚ 2011‚ p. 15). Found generally in alcoholics‚ the combination of their compromised metabolism and thiamine deficiency results in Wernicke’s Encephalopathy‚ which then progresses to Korsakoff’s syndrome (Thompson‚ Guerrini
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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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For Paragon Tool CEO Nicky Anaptyxi‚ concerns over the potential acquisition of MonitoRobotics are certainly warranted. The board‚ hired consultants and even Nicky himself appear to be completely split on the decision. From case facts‚ there are three possible courses of action for Paragon Tool: (1) acquire MonioRobitics to accelerate the development of manufacturing service software and ward off competitor Bellow & Samson; (2) forego the acquisition and organically grow the company’s own
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Forensic Tools: Redline Vs. Volatility One of the hardest choices to make when dealing with a problem is‚ what tool will resolve this issue? There are hundreds of tools that deal with the different aspects and approaches to memory forensics and incident response. Failing to choose a tool‚ leaves a hole in mission related capabilities. The two that are discussed within this paper are Redline and Volatility. These tools address the issue of memory forensics and incident response; however‚ they take
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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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Charge Syndrome Introduction Charge Syndrome is a specific collection of non-randomly occurring congenital anomalies. The acronym CHARGE actually stands for the major features of this syndrome. The letter C stands for coloboma of the eye‚ H is heart defects‚ A stands for atresia of the choanae‚ R is retarded growth and development‚ G stands for genital abnormalities and lastly letter E stands for ear anomalies and/deafness. The cause of this syndrome may be genetically heterogeneous‚ but
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Rett Syndrome Abstract Rett syndrome is considered one of the autism spectrum disorders. Rett syndrome is a developmental disability disorder resulting in severe mental and physical deficits in female children. Rett syndrome is grouped as a pervasive developmental disorder (PDD) in which conditions are severe and pervasive‚ and that begin in early life and influence multiple areas of development. Rett syndrome‚ including the age of onset and the severity of symptoms‚ varies from child to
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