Jacob Santel Mrs. Potter Reading Down Syndrome(Need different title) This is one of the most interesting genetic diseases in the world‚ and yet there is no cure for it. This disease can affect people drastically‚ or sometimes very little at all. Although there is no way to treat it‚ it can be helped‚ and there are many programs to help. This complex genetic disease is called down syndrome. Down Syndrome has many effects. People with down syndrome usually “look alike.” They usually have a
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Stockholm syndrome and posttraumatic stress disorder. And‚ you know‚ I had no free will. I had virtually no free will until I was separated from them for about two weeks” (Patty Hearst). In 1974‚ Patty Hearst developed Stockholm syndrome after being kidnapped by an American communist group. She was dependent on her kidnappers and felt secure with them. Because of this‚ she followed the beliefs of the group and performed terrible tasks with her kidnappers. By definition‚ “Stockholm syndrome is a condition
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Imagine you are a person living with Lynch Syndrome‚ this means you have an 80% chance of developing numerous kinds of cancer. Lynch syndrome is a genetic disorder caused by a group of mutations that greatly effect a person to an early and aggressive stage of colon cancer. Although this genetic mutations can cause other cancers‚ colon cancer is most common. The main cause of Lynch syndrome is miss-matched genes. This genetic disorder is passed down from parents on the MLH1 gene on the third chromosome
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Rett Syndrome: Important to Diagnose Imagine this‚ you are enjoying the Christmas holiday at your grandparents with your aunts‚ uncles‚ and cousins. You think nothing of it because it is a completely normal thing to do. This is the first year all of my cousins were together in about three years. I introduced my boyfriend‚ Devin‚ to my other cousins he hadn’t met yet. As we were talking‚ I grabbed a plate of snacks when my five year old cousin walks up to me. She did not say anything just stared
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easier time diagnosing Asperger syndrome disorder. The percentage of misdiagnosing Asperger syndrome disorder would lower with the correct equipment that tells the accurate diagnoses. Medical experts have misconceptions about Asperger syndrome‚ which leads to misdiagnosing the behavioral and mental state that would result in the patients’ not getting proper treatment. Within the community; Citizens and medical experts have misconceptions about Asperger’s Syndrome. For example citizens
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and many aweing theories arguing if Abraham Lincoln had a disorder called Marfan syndrome or not‚ which was eventually resolved when Lincoln actually inherited a disease called Multiple Endocrine Neoplasia Type 2B. Contributing to the dispute of Marfan syndrome in Abraham Lincoln‚ in 1964 a physician published his findings and observations in the Journal of the American Medical Association which diagnosed Abraham Lincoln that he had Marfan syndrome (Kugler). However‚ his conclusions were eventually
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Stickler’s Syndrome Stickler’s Syndrome is a connective tissue disorder that causes problems with vision‚ hearing‚ bones‚ and joints. Stickler’s Syndrome was named after Dr. Gunnar B. Stickler. In 1960‚ a 12 year old boy was analyzed at Mayo Foundation in Minnesota. The boy had expansions of quite a few of the joints‚ he was also very short sighted. His mother also had a problem‚ she was blind. Dr. Stickler founded that other members of this family had similar symptoms. This made Stickler
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Genetic Project: Down Syndrome What is Down Syndrome? Down Syndrome is a chromosomal disorder where a child is born with an extra partial or full chromosome 21‚ thus leading to the over-expression of many genes present on this extra chromosome. Therefore‚ it is neither dominant nor recessive. Down Syndrome affects about 1 in 700 babies born‚ making it one of the most common genetic birth defects in the United States. There are actually 3 different types of Down Syndrome‚ Trisomy 21 (Nondisjunction)
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A Case Study on Compartment Syndrome of the Forearm in a soccer player Objective: To describe the evaluation‚ diagnosis‚ and current treatment of a men’s soccer player with compartment syndrome of the forearm. Background: The forearm is the most common site for compartment syndrome in the upper extremity. The compartments of the forearm include the volar (anterior or flexor)‚ and the dorsal (posterior or exterior). Both bone forearm fractures and distal radius fractures are common initial
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Robert’s Syndrome or Psuedo Thalidomide Syndrome is a gentic disorder with many growth delays before and after birth. This syndrome shows the malformation of legs and arms‚ abnormalalitles of the skull and facial regions. In most cases‚ it causes intelutcal disabitlly. In a case presneted‚ the parents of four children‚ the third conception had Robert’s Diesase. However the child was not diagnosed till the age of two. The only sign at birth was a cleft palate. At the age of two‚ the child was unable
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