Creative Title: Tay-Sachs‚ the saddest of diseases Introduction: Tay-Sachs disease (TSD) is a genetic condition affecting male and female infants. The life expectancy of children with TSD is just 3-4 years old. Unfortunately‚ it is always fatal and there no known cure. What is the cause of the disease and how is it inherited? Tay-Sachs disease is hereditary‚ meaning it is inherited from family members. TSD is the result of an autosomal recessive gene‚ meaning‚ meaning that two copies of an abnormal
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Denita LaRock HCA/240 January 21‚ 2013 Crohn’s Disease Nakki Price Crohn’s disease is an inflammatory bowel disease that affects the bowel tissues. The inflammation begins in the lining of the digestive tract‚ and may spread into the layers of the bowel tissue. This disease causes severe diarrhea‚ abdominal pain‚ and malnutrition. Other symptoms are ulcers‚ fever‚ weight loss and reduced appetite. Abdominal pain‚ blood in stool‚ and unexplained diarrhea or fever lasting more than two days
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Inflammatory bowel disease affects about one million Americans. Crohn ’s disease and ulcerative colitis are both types of irritable bowel disease‚ or IBD. Crohn ’s disease is an ongoing illness that creates inflammation in the walls of the digestive tract. It can affect any area of the gastrointestinal tract (GI)‚ from the mouth to the anus. Although it can be found along any part of the GI tract‚ it is most commonly detected in the small intestine. This paper will highlight the history‚ causes
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A rare and fatal disease‚ Tay-Sachs is characterized as one of the devastating neurodegenerative disease. Children afflicted with Tay-Sachs “lose motor skills and mental functions” eventually becoming “blind‚ deaf‚ mentally retarded‚ paralyzed...Tay-Sachs children usually die by age five” (“Tay-Sachs Disease”). A diagnosis of infantile Tay-Sachs is akin to a death sentence; the only form of care would be comfort for death. Tay-Sachs is passed on genetically from parent to child and‚ as it is an autosomal
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Ingersoll Mrs. Scanavino BIO 209-S9 19 Mar. 2012 An Examination of Parkinson’s Disease and its Effects Through the study of anatomy and physiology‚ physicians have learned that Parkinson’s disease can be developed many ways‚ include many symptoms leading to diagnosis and although incurable can be treated and managed. According to the National Institute of Neurological Disorders and Strokes‚ Parkinson’s is a disease related to the loss or underactive production of dopamine producing brain cells
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References • http://www.thefreedictionary.com/hereditary+disease • http://en.wikipedia.org/wiki/Pathogen • http://www.preservearticles.com/201101032353/deficiency-diseases.html • http://www.who.int/chp/working_paper_growth%20model29may.pdf • http://www.drugs.com/condition/pneumonia.html • http://www.medicinenet.com/diabetes_treatment/article.htm • http://www.nhlbi.nih.gov/health/health-topics/topics/asthma/treatment.html • http://en.wikipedia.org/wiki/Haemophilia
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Introduction to Parkinson’s disease Parkinson’s disease is a chronic progressive movement disorder. It happens when nerve cells in the brain don’t produce enough of a brain chemical called dopamine. Parkinson’s disease was founded by a doctor in London in1817 name James Parkinson. He wrote a book called the “shaking palsy” that he researched in his neighborhood to find out where the disease came from Weintraub‚ D. (2008)” Dopamine and shaking palsy in “Parkinson’s disease” Practical Neurology 80(4);110-125
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Parkinson’s Disease has been around since ancient times and man have been aware of the disease since then. In western Medicine a physician named Galen described Parkinson’s as “shaking palsy” in AD. 175. A thorough medical essay was published about the “shaking palsy” in 1871 by London doctor James Parkinson. The disease was named after Parkinson and his essay was called “An Essay of the Shaking Palsy.” The essay paved the way for parkinson’s and established it as medical condition. Parkinson’s
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Huntington ’s disease John Doe HCS/245 10/20/2013 Prof Jane Huntington ’s disease In 1993 researchers discovered the gene that causes Huntington’s disease. (Huntington ’s disease Society of America‚ 8/27) Huntington’s disease is a disease which progressively degenerates cells in the brain slowly over time. Since the nerve cells in the brain are slowly dying it causes uncontrollable movements‚ emotion changes and other forms of determination of psychological aspects. (The Diagnosis and
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Communicable Disease * Keep in mind all have fever‚ swollen LN‚ rash etc. Scarlet Fever: * Cause: Group A beta Hemolytic Streptococcus * Spread via direct contact/droplet * May lead to RF * Uvula/pharynx beefy red; tonsils have white exudate‚ pinpoint lesions on palate * Sandpaper rash * Pastina Sign: hyperpigmentation at joints * TONGUE (white furry white strawberry strawberry ) * So throat culture if they have strept/sore throat *** Anybody with a sore throat
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