Marfan Syndrome Wesley Thompson Jim Hutchins Biomedical Core 1110 November 19‚ 2011 Marfan syndrome is a variable‚ autosomal-dominant disorder in the connective tissue with distinct physical characteristics. The principal features affect the cardiovascular system‚ eyes and skeleton. This condition affects the connective protein that forms the structural support for tissues outside the cell. This disease is a result of a faulty makeup of chromosomes. Since MFS (Marfan Syndrome) is an
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Metabolic syndrome Insulin resistance syndrome; Syndrome X Last reviewed: June 2‚ 2012. Metabolic syndrome is a name for a group of risk factors that occur together and increase the risk for coronary artery disease‚ stroke‚ and type 2 diabetes. Causes‚ incidence‚ and risk factors Metabolic syndrome is becoming more and more common in the United States. Researchers are not sure whether the syndrome is due to one single cause‚ but all of the risks for the syndrome are related to obesity. The
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Piaget insisted that cognitive development followed a sequence and that stages cannot be skipped and that each stage is marked by a new intellectual abilities and a more complex understanding of world by children ‚ then experience discrepancies between what they already know and what they discover in their environment. The goal of this theory is to explain the mechanism and processes by which the infant ‚ and then the child develops into an individual who can think using hypothesis . According
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In this imbalance research paper‚ it will discuss and explain of a certain disorder in the nervous system called Tourette’s syndrome. It will also acknowledge the current studies and research that can potentially find a way to cure this disorder. First‚ we need to more knowledgeable about this disorder. Tourette’s syndrome “is a nervous system (neurological) disorder that starts in childhood. It involves unusual repetitive movements or unwanted sounds that can’t be controlled (tics)” (Mayo Clinic
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Cushing Syndrome Sometimes called hypercortisolism. Cushing s syndrome is a hormonal disorder caused by prolonged exposure of the body s tissues to high levels of the hormone cortisol. Causes Pituitary Adenoma Pituitary adenomas cause 70 percent of Cushing s syndrome cases‚ excluding those caused by glucocorticoid use. These benign‚ or noncancerous‚ tumors of the pituitary gland secrete extra ACTH. Most people with the disorder have a single adenoma. Ectopic ACTH Syndrome Some benign
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Tourette Syndrome is a neurological disorder that is characterized by sudden repetitive and involuntary movements or vocalizations that are generally termed “tics”. These tics can have different degrees of intensity ranging from simple to complex. Simple motor tics are brief‚ sudden‚ and repetitive movements that involve a limited number of muscle groups. They include facial grimacing‚ eye blinking and other eye movements‚ and head or shoulder jerking. Simple vocalizations include repetitive sniffing
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When comparing the work of Piaget and Vygotsky‚ thought is given about the profound impact their theories have made on child development and learning. It is interesting how they both approached this topic from different perspectives and emphasized different methodologies. Educators‚ scholars‚ and parents have used their philosophies to understand how children learn and to create strategies to teach them. While their theories do share some similarities‚ there are some differences. Piaget’s theory
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Ophelia Syndrome Study Skills November 12‚ 2012 In the essays of Diagnosing and Treating Ophelia Syndrome and Everybody is Ignorant on Different Subjects two topics are discussed which are related‚ in that they both have to do with learning and being able to think as an individual. The Ophelia Syndrome is not processing the ability to create one’s own opinion. Ophelia is a character in the play Hamlet. She is described as a helpless child and has a “Lord” or authoritative figure that forces
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01/29/2003. The SSA granted disability benefits because of borderline intellectual functioning and pervasive developmental disorder. She had a history of Apert’s syndrome
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Marfan’s Syndrome Marfan syndrome is an inherited connective-tissue disorder transmitted as an autosomal dominant trait. It is distributed worldwide‚ has a high prevalence rate and has pleiotropic manifestations‚ meaning one gene influences multiple traits that do not seem to be related. Mutations of the FBN1 gene on the 15th chromosome (more specifically chromosome 15q21.1) cause Marfan syndrome. The FBN1 gene is coded to make a glycoprotein called fibrillin-1
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