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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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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Battered wife syndrome (a condition created by sustained physical‚ sexual‚ and/or emotional abuse‚ which creates a variety of physical and emotional symptoms) has been used as a defence in murder cases in which women have killed or harmed their abuser. Although expert testimony regarding battered wife syndrome has gained some acceptance in the courts‚ it is questionable that it provides enough solid and substantive evidence to be used as a credible defence. The battered wife syndrome defence is more
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full productive life. What is Autism? Autism is a developmental disability‚ also known as a Neurobiological disorder‚ that effect 1 in 1000 children. Neurobiological Disorders are genetic‚ metabolic‚ or involve other biological factors. Disorders such as‚ bi-polar‚ autism‚
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WK #7 Final Project: Needs Analysis Essay Blake Urquhart Professor Johnson SPHE 314: EXERCISE PHYSIOLOGY As kids begin playing competitive sports at earlier and earlier ages so to does the demand for training‚ and sport specific training seems to be at an all time high. However while trainers are great for helping in the category of weight loss or better overall health they often times do not have the tools
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Thoracic Outlet Syndrome (TOS) is used to describe upper extremity symptoms and according to recent reports 1‚2 is defined as compression of the neurovascular structures in the interscalene tri-angle‚ as it exits the thoracic girdle. The bony anatomy of thoracic outlet‚ which will be discussed in further detail‚ can be defined by the space between the first thoracic vertebra‚ first rib‚ and manubrium of the sternum.1 Thoracic Outlet Syndrome is not specific in determining the struc-ture being compressed
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MSSW JAYWANT [] Acute coronary syndrome is a term used for any condition brought on by sudden‚ reduced blood flow to the heart. Table of Contents ACUTE CORONARY SYNDROMES IN OLD AGE. DEFINITION Acute coronary syndrome is a term used for any condition brought on by sudden‚ reduced blood flow to the heart. Acute coronary syndrome symptoms may include the type of chest pressure that you feel during a heart attack‚ or pressure in your chest while you’re at rest or doing light
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The Appellant’s primary diagnosis is Down’s syndrome. The services provided through the Independence HCBS waiver would require the Appellant to have three (3) or more limitations in daily living‚ self-care‚ mobility‚ communication‚ or self-direction however‚ an eligible applicant would require hands
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most common type of deaf-blindness disease in the world is Usher Syndrome. Usher Syndrome is a clinically and genetically heterogeneous disease. It is inherited in an autosomal recessive inheritance pattern. Worldwide‚ the chance of a baby being born with Ushers Syndrome is approximately 1 in every 25‚000 babies. To date‚ there are roughly 50‚000 people with Ushers Syndrome living in the United States. As stated above‚ Ushers Syndrome is an inherited disease characterized by hearing impairment and
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