Erythrocyte sedimentation rate

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    Rheumatoid Arthritis Jacob Elisha Carrington College Immunology 09/17/2015 Rheumatoid Arthritis Living on this Earth, humanity may encounter many different viruses, and infectious diseases which have the potential to jeopardize a well-being. In regards to autoimmune diseases, these types of conditions are due to your body’s immune system fighting off its own self. One of the more unfortunate autoimmune diseases attacks joints, and it is called Rheumatoid Arthritis. This disease can cause

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    Rheumatoid Arthritis A 60-year-old female was admitted to Winter Park Florida Hospital for cellulitis. A radiographic examination of both ankles was ordered. While taking images of the patient’s ankles, these images clearly showed that there was a decreased in bone density. When the technologist and I talked to the patient, we found out that the patient had been diagnosed with rheumatoid arthritis since she was 25 years old. After reading the radiologist’s report, we noticed that the radiologist

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    Chapter 65: Nursing Management: Arthritis and Connective Tissue Diseases Test Bank MULTIPLE CHOICE 1. Which finding will the nurse expect when assessing a 58-year-old patient who has osteoarthritis (OA) of the knee? a. Discomfort with joint movement b. Heberden’s and Bouchard’s nodes c. Redness and swelling of the knee joint d. Stiffness that increases with movement ANS: A Initial symptoms of OA include pain with joint movement. Heberden’s nodules occur on the fingers. Redness of the joint is more

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    Case Presentation: An otherwise healthy 9-month-old boy was brought to the Emergency Department by respite foster parents with a chief complaint of unusual bruises and marks on his skin. Two days prior to the ER visit, the respite foster parents had noticed some left eye redness and swelling, which by day of presentation had progressed to a large swollen blue-black lesion on his left cheek and new scattered bluish lesions on his thighs. The child had been diagnosed with a viral upper respiratory

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    Fatal Insomnia Synthesis

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    Abstract Fatal insomnia, categorized as either familial or sporadic, is an acknowledged rare form of prion disease. Patients express progressively debilitating symptoms which include insomnia, dysautonomia, endocrine disturbance, cognitive dysfunction, and motor abnormalities. A distinct feature of fatal insomnia is the selective atrophy of the thalamus. This and other known cellular changes in fatal insomnia illuminate the diverse functionality of particular brain areas. Similar symptomatic complications

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    more than 6 criteria = definite RA. • Disease activity was assessed with the 28-joint disease activity score (DAS28). Routine Laboratory investigation: • Complete blood picture was done for healthy and RA patient groups. • The erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP) will be done. • Rheumatoid factor (RF)-IgM was determined in all patients by means of latex agglutination. • Serum levels of anti-cyclic citrullinated peptide (anti-CCP) were measured by ELISA. Concerning

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    RUNNING HEADER: KAWASAKI DISEASE​​Dinesh 1​​​​ Kawasaki Disease Rekan Dinesh Mrs. Cheryl Taylor Southeastern College Abstract Kawasaki disease is a disease that predominately affects children. It is a condition that causes an inflammation of walls of arteries. The disease is very rare, so rare that there are fewer than 20,000 cases per year in the United States. Due to its rarity, the etiology of the disease is unknown, causing the medical diagnosis of the disease

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    Case presentation and history Michael is a 12 years old boy who is a slim built and he is attending year seven at a local High school for visual Arts and Design. Michael is living with his mother, father, and younger brother. Michael has presented symptoms of severe stress, moderate mood, and normal anxiety during the last week before the assessment. Michael has a history Obsessive Compulsive Disorder and he indicated fears of harming other, resulting in checking and reassurance behaviour as well

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    Acute Lupus Pneumonitis

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    Interstitial lung disease is much less common in SLE, being more frequent as disease duration increases. Nonspecific interstitial pneumonia is the most common histological pattern found in patients with SLE (Torre and Harari, 2011). Acute lupus pneumonitis is a rare manifestation of lupus, with an incidence ranging between 1-12%. Patients with acute lupus pneumonitis usually present with fever, dyspnea, cough, tachypnea, and pleu¬ritic chest pain. Physical findings commonly include basal crackles

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    Patients and methods This is a longitudinal cross sectional study of all children and adolescents patients with LN following inPediatric Allergy and Immunology clinic, Children 's Hospital, Ain Shams University in the period between October 2013 and February 2014. Lupus nephritis in patients with pediatric onset SLE was diagnosed and graded on pathological basis according to 2003 ISN/RPS classification of LN into Class I: Minimal mesangial LN. Class II : Mesangial proliferative LN. Class III: Focal

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