"Down syndrome care plan" Essays and Research Papers

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    Pathophysiology Teaching Plan to Enhance Self-Care Kelianna Karnatz University of Mary Pathophysiology Teaching Plan to Enhance Self-Care Patient confidence in managing their care is fundamental in successes of the patient’s care. The ability to cope with not only the diagnoses of diabetes but also be able to manage the life adjustments which requires daily attention is a challenge which needs assistance from health care providers. Diabetes Diabetes has two types‚ Type 1 which had been known as

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    Hypertrichosis: The Werewolf Syndrome The disease Hypertrichosis‚ also known as “The Werewolf Syndrome‚” causes unwanted/abnormal hair growth either in one spot or all over an affected person’s body. There are two main types: Naevoid‚ and Congenital. Naevoid Hypertrichosis‚ is where the hair grows in one spot on the body‚ sometimes the limbs but usually proportional in the facial area. Congenital is where hair covers a majority of the body‚ sometimes right after birth! In severe cases‚ the

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    general adaptation theory (GAS).  [pic] The General Adaptation Syndrome (GAS)  In order to develop a general theory for the physiological response of humans and animals to stress‚ Hans Selye‚ former director of Experimental Medicine and Surgery at the University of Montreal‚ performed an integrated analysis of the effects of stress on adrenal gland function. He called his model of stress adaptation the General Adaptation Syndrome or GAS. The GAS was thought by Selye to outline how the organism

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    Budd Chiari Syndrome

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    advantages and disadvantages? Budd Chiari Syndrome •Clinical term used to describe the manifestation of hepatic venous outflow obstruction •Secondary to hepatic vein thrombosis •Or to the narrowing/occlusion of the inferior vena cava (Khan 2009‚Val DC 2003) Ostial stenosis web thrombus Abdominal vein Liver Stomach Gallbladder Enlarged caudate lobe Inferior vena cava Portal vein (Menon et al.‚ 2004) Budd Chiari Syndrome • Primary type -Endoluminal venous (I.e. Thrombosis

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    Polycystic Ovarian Syndrome The most common female endocrine disorder is Polycystic Ovarian Syndrome (PCOS). As reported by the Polycystic Ovarian Syndrome Association‚ PCOS is the imbalance of hormones in a women’s body which can lead to menstrual cycle changes‚ cysts in the ovaries‚ trouble getting pregnant‚ and other health changes (What is PCOS‚ 2009). The cause of this endocrine disorder is unknown‚ however‚ according to the National Institute of Health (NIH)‚ it is connected to changes in

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    Angelman Syndrome Essay

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    Diarmuid Sugrue Angelman Syndrome SYMPTOMS Angelman Syndrome is a neuro-genetic disorder involving the chromosomal region 15q‚ between positions 11-13. The symptoms primarily include intellectual development retardation‚ epilepsy‚ speech impairment‚ ataxia‚ and persistent laughing or smiling. CAUSATIVE MUTATIONS A healthy individual receives 2 copies of the 15 chromosome‚ one maternal and one paternal. The chromosomal region 15q11-13 (base pairs 23‚133‚488-23‚235‚220)‚ contains the gene

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    Patau syndrome essay

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    Patau syndrome is a disorder that occurs due to the appearance of a person’s thirteen chromosome three times (trisomy 13) instead of only twice in the cell. In some cases of the disorder‚ only a select percentage of the cells display the third thirteen chromosome while others contain the average amount of pairs‚ this is known as mosaicism. The extra chromosomal material in the cell can lead to many problems in the developmental stages of the humans life‚ these developmental issues cause severe mental

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    A Long Way Down

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    Suicide and humor are two words not often associated with each other‚ but Nick Hornby takes the pair on in his novel A Long Way Down‚ a dark comedy about suicide and life after a failed attempt. The book is narrated by four characters taking turns telling the story in their voice. The resulting hodgepodge gang includes Martin‚ a quasi celebrity who loses everything after an affair with a fifteen-year old girl; Maureen‚ the middle-aged mother of a severely disabled son; Jess‚ an obnoxious teenager

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    Williams Beuren Syndrome

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    Williams-Beuren Syndrome: Controversies in the Complex Behavioral and Cognitive Profile of a Unique Genetic Disorder Zachary Blaker November 12‚ 2015 (3‚982 words) Introduction Williams-Beuren Syndrome (WBS) is a rare neurodevelopmental disorder typically characterized by distinctive facial features‚ cognitive delays accompanied by comparatively strong language and verbal skills‚ deficits in visuospatial construction‚ and hyper-social personality traits (Martens et al. 2008)

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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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