| Genetics Disease Brochure Assignment | ||||||||||||||||||||||||||||
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Genetic Disorder Brochure Project Overview Create a tri-fold brochure for a doctor’s office waiting room. The brochure should provide patients with information about one of the genetic disorders listed below. Assume that most of the patients of your audience are adults with a typical high school science background. The brochure should be creative as well as informative. You want people to pick it up and read through it. Be sure to include accurate, up-to-date information and graphics that illustrate important ideas. You should reference at least four sources of information on a separate “works cited” page to hand in along with your brochure. (Google DOES NOT count). If you need a hard copy of the assignment, click here. Procedure You will research the genetic disorder of your choice and use the following questions. as a guide, to the type of information you will need for your brochure.
Brochure After researching the disorder, make an informational pamphlet that could be given to patients. The pamphlet must be no larger than 8.5 x 11 unfolded. This brochure should be of professional quality. It must fully inform the reader of all issues pertaining to the genetic disorder. Again, use the questions provided to guide your research. Your brochure will be graded based on accuracy, completeness, and creativity. Visual representations (pictures, graphs, etc.) should be incorporated into the brochure. Give credit for graphics you did not make. Works Cited Page You will need to prepare, on a separate sheet, a works cited page that identifies all sources used to make the brochure. At least four sources are required for this project. More than four is acceptable, and encouraged! (Be sure to use proper format; do not just list websites, list author, title, date, etc.) Here is an example of how you record your reference:
Possible Internet Resources (use google.com to find other sites)
List of Genetic Diseases *Prader – Willi Syndrome *Marfan Syndrome *Angleman Syndrome *Cat Eye Syndrome *Cystic Fibrosis *Hemophilia A *Huntington’s Disease *Fragile X *Tay Sachs *Sickle Cell Anemia *Neurofibromatosis I or Von Recklinghausen Disease *Cri-du-chat or Cat’s Cry Syndrome *Wolf Hirschhorn Syndrome *Monosomy 9p or Alfi’s Syndrome *Jacobson Syndrome *Smith- Magenis Syndrome *Patau Syndrome or Trisomy 13 * Edwards Syndrome *DiGeorge Syndrome *PKU *Rentinitis pigmentosa *Burkitt’s Lymphoma *Albinism, ocular, x-linked, type 1 *Duchenne Muscular Dystrophy *Fabry Disease *Hemophilia B *Adrenoleukodystrophy *Myotonic Dystrophy or Steinert Disease *Neurofibromatosis *Rett Syndrome *Von Hippel-Lindau Syndrome *Albinism, oculocutaneous, type 1 *Dyslexic Specific-1 or Primary, word blindness, Congenital reading disability *Alzheimer disease, familial, type 5 *Down Syndrome or Trisomy 21
Genetics Brochure Rubric
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