"Empty nest syndrome" Essays and Research Papers

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    Overview Diabetic hyperosmolar syndrome is serious complication that is sometimes experienced by diabetic patients‚ most commonly those with type 2 diabetes. It occurs when the body consistently produces dangerously high blood sugar levels. As a result‚ the body attempts to flush out the excess blood sugar through increased urination. If it is not treated‚ it can become life threatening or even fatal. While the condition often develops in response to an infection or illness‚ it can also be caused

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    Tumor Lysis Syndrome

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    Tumor Lysis Syndrome by NinjaMom Tumor Lysis Syndrome is a series of metabolic derangements which may begin shortly after the onset of treatment of malignancies. It can lead to any of the following: · hyperphosphatemia · lactic acidosis (metabolic acidosis) · hypocalcemia · hyperuricemia · hyperkalemia · acute renal failure Tumor Lysis Syndrome (TLS): · is caused by the destruction of many rapidly proliferating neoplastic cells · is most commonly associated with

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    Restless Legs Syndrome

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    Restless Legs Syndrome I. History of Disorder Restless legs syndrome is a neurological disorder that has been studied for hundreds of years. The earliest documentation of the syndrome was recorded nearly 400 years ago by Thomas Willis‚ a 17th century English physician who served King Charles II. Willis described cases of people having trouble sleeping because of constant contractions of tendons in the legs. Soreness resulted from these contractions and would hinder sleep for days at a time. The

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    Ehlers-Danlos Syndrome

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    Ehlers-Danlos Hypermobility Type: Pathophysiology and Treatment Abstract Ehlers-Danlos syndrome is a degenerative condition caused by the malformation of collagen within the body. Many different types of Ehlers-Danlos syndrome have been linked to different types of collagen malformation in different tissues. Hypermobility type Ehlers-Danlos syndrome (HT-EDS) is the most common type of Ehlers-Danlos syndrome. HT-EDS is mainly characterized by marked joint instability and mild cutaneous involvement

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    Accessory navicular syndrome involves an extra piece of either cartilage or bone located on the medial side of the foot‚ on the navicular bone. The accessory navicular articulates with the navicular bone‚ while the navicular bone articulates with numerous bony structures. It articulates posteriorly with the talus‚ anteriorly with the cuneiform bones‚ and laterally with the cuboid bone. The joint associated with accessory navicuar syndrome is the talonavicular joint (Panchbhavi‚ V. K.‚ 2015‚ December

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    Student: Eibhlín Ní Mhuircheartaigh ID Number: 59210388 Qualification: M.Sc. Guidance & Counselling Module: ES551: Wellbeing‚ Society and Lifelong Learning Title of Essay/Seminar Paper: Case Study: School struggles of those living with Asperger Syndrome Please indicate the term and academic year this module was studied: Spring 2010 Term: Autumn  Spring Summer Academic Year: 2009/2010 Is this a re-submission? Yes  No Word length: 2‚735 Date of

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    Tourette Syndrome Analysis

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    Overview Tourette Syndrome (TS)‚ also named multiple tics-coprolalia syndrome‚ was initially described by Gilles de la Tourette in 1900. It is a “developmentally regulated neurobehavioral disorder characterized by multiform‚ frequently changing motor and phonic tics.” (Brunn‚ Cohen‚ &Leckman‚ 2012) Tics means “involuntary‚ rapid repetitive and stereotyped movements of individual muscle groups.” (Brunn‚ Cohen‚ &Leckman‚ 2012) Although the definite cause of TS is unknown‚ it is well recognized that

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    Prader-Willi Syndrome

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    Prader-Willi Syndrome Prader-Willi Syndrome is an unusual disorder rooting from the gene that is passed down to that person (Prader-Willi Syndrome). This disorder can act as an origin for a perpetual sensation of hunger as well as weak muscle tone and a minimal amount of sex hormones (Prader-Willi Syndrome) .This disorder is generally caused by the lacking pieces or defect in chromosome 15 in addition to the malfunction in the part of the brain that controls hunger.. Unfortunately‚ PWS

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    Parental Alienation Syndrome or PAS is a condition named conceived by the late Richard Gardener MD in the late 1980’s. It is described by Gardener as: a disorder that arises primarily in the context of child-custody disputes. Its primary manifestation is the child’s campaign of denigration against the parent‚ a campaign that has no justification. The disorder results from the combination of indoctrinations by the alienating parent and the child’s own contributions to the vilification of the alienated

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    Stevens Johnson Syndrome

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    complications to occur. While many of the potential side effects and complications that can arise with medications are minor or uncommon‚ there are others that can be very serious and have potential for mortality. Stevens Johnson Syndrome (SJS) and Toxic Epidermal Necrolysis Syndrome (TENS)‚ are both a form of a very serious and rare skin disorder‚ that could result in death‚ due to adverse drug reactions. This disease affects the skin and mucous membranes‚ in which the layers of the skin start

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