What a Diagnosis of Down Syndrome Means Today Down syndrome is a condition affecting many Americans and individuals across the world. It presents challenges socially‚ academically‚ and behaviorally. However‚ a diagnosis today is not nearly as detrimental to the person’s quality of life as it was decades ago. Strides have been made in Down syndrome awareness‚ education and overall acceptance. Screening is now available so that parents know in advance if they are going to have a child born with
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Marfan syndrome is a genetic disorder that affects the body’s connective tissue. Connective tissue connects all the organs‚ tissue and body cells together. It also plays an important role in helping the body grow and develop properly. People are born with Marfan Syndrome but they may not notice it until their teen years. The signs and the symptoms of the Marfan syndrome varies. They are so different‚ that people can have the same disease bt they can different symptoms. And with that being said‚ they
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Prader-Willi Syndrome: An Investigation into Paternal and Maternal Origins & Characteristics Abigail McNeal Liberty University COUN 502- Professor Myers August 15‚ 2011 Abstract Prader-Willi syndrome‚ (PWS) is a genetic disorder that occurs in about one in every eight thousand births in the United States. PWS occurs when there is a defect or deletion in the fifteenth chromosome from either maternal or paternal origins. Individuals diagnosed with PWS need enhanced supervision to address the
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Down Syndrome Down Syndrome is a chromosomal disorder. It occurs in about 1 of every 800 births. People with Down syndrome may have mild to severe learning disabilities. Physical symptoms include a small skull‚ extra folds of skin under the eyes‚ and a protruding tongue. People with Down syndrome are subject to a variety of medical problems including heart abnormalities and thyroid gland dysfunction. Survival rates have been increased dramatically in recent years as problems specific to Down syndrome
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read and am aware of the university requirements regarding academic honesty." Should the battered woman syndrome be admissible as a murder defense in American courts and should expert testimony be permitted on such a syndrome? Since the 1970’s when the battered woman syndrome was first proposed by Dr. Lenore Walker‚ women have been using this syndrome to proclaim mental illness due to the syndrome aligned with self-defense as an excuse for their crimes (Dixon‚ 2001). Dr. Walker defined the battered
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Aspergers Syndrome is a lifelong neurobiological disorder of social interaction and behavior (Frith 2004; Wing 1981; Gillberg and Gillberg 1989; Klin et al. 2000). The purpose of this study was to study the language performance in school-aged children with Aspergers Syndrome along with their age‚ sex‚ and IQ matched controls. Prior to the study‚ they expected children with Aspergers Syndrome to perform below average in the selected measures of language due to their difficulties in language development
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Chromosomal Disorder: (Turner Syndrome) Introduction Turner Syndrome is a condition that only alters the development of girls and women. Most girls and women have two full and complete X chromosomes while girls with turner syndrome have only part of the second X chromosome. Women and girls are diagnosed with turner syndrome have features such as slow growth rates‚ a webbed neck‚ broad shoulders‚ and widely spaced nipples. They also have swelling hands and feet‚ heart defects‚ kidney problems‚ and
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The history and background of marfan disease. Marfan syndrome (MFS) is an inherited connective tissue disorder noteworthy for its worldwide distribution‚ relatively high prevalence‚ and clinical variability. This autosomal dominant syndrome has pleiotropic manifestations involving primarily the ocular‚ cardiovascular‚ and skeletal systems. Classic marfan syndrome MFS type 1‚ MFS1 has been considered a condition caused by the deficiency of a structural extracellular matrix protein‚ fibrillin-1; however
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I found this reading pretty interesting actually. I had never heard much on Tourette’s syndrome‚ let alone the history of how it came about. Personally‚ I did not know what kinds of symptoms must be present in order for one to be diagnosed with Tourette’s. The story that was told of the man whose name was Ray‚ I found to be most interesting. Throughout the story‚ you could tell that he was not happy with the medicine he was receiving to help control his symptoms. He became angry because of the loss
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EHLERS DANLOS SYNDROME WHAT IS THE EHLERS DANLOS SYNDROME? • EDS is a group of rare inherited disorders • The disorder weakens connective tissues • Connective tissues support joints‚ blood vessels‚ skin and other organs • There are 6 major types of EDS • Different types are classified according to appearance of signs and symptoms. – Hypermobility – Classical – Vascular – Kyphoscoliosis – Arthrochalasis – Dermatosparaxis WHAT ARE THE SPECIFIC SYMPTOMS? • Overly flexible joints • Hypermobility
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