Presentation on theme: "By: Breanna Parker & Jake Perkins. Sickle Cell History In 1910 Sickle Cell Anemia was discovered by James B. Herrick. James was running blood tests."— Presentation transcript:
By: Breanna Parker & Jake Perkins
Sickle Cell History In 1910 Sickle Cell Anemia was discovered by James B. Herrick. James was running blood tests on a patient and he noticed unusual characteristics in the shape of the blood cells. He noticed the blood cells were in the shape of a moon instead of a circle. Sickle Cell Anemia is more commonly in people who have ancestors from sub-Saharan Africa. http://www.sciencedaily.com/rele ases/2010/11/101102130133.ht m
Sickle Cell Description Sickle cell anemia is an inherited blood disorder. The red blood cells are in the shape of a moon instead of a circle. It effects a persons immune system and they are unable to fight off infections as fast as the average person. http://www.medicinenet.com/si ckle_cell/article.htm
Symptoms Fatigue Paleness Shortness of breath Yellowing of eyes and/or skin at birth; jaundice. Delayed puberty Eye problems Abdomen and joint pains Low immune system Someone with sickle cell can live a full, healthy life however, depending on the severity of your sickle cell your life expectancy can range from 40-60 years old.
Area of Body Targeted The immune system and blood stream are mainly effected by this disease. Children and adults with sickle cell are more vulnerable to infections and have a harder time fighting them off. http://evadianita.com/wp- content/uploads/2011/02/Sickle-Cell- Anemia.jpg
How it is Genetically Transmitted Two defective genes (SS) is needed for a child to be diagnosed with sickle cell anemia. If each parent carries one defective gene (S) and one normal gene (A), each child has a 25% chance of inheriting two defective genes and having sickle cell anemia and a 25% chance of inheriting two normal genes and not having the disease, also have a 50% chance of not being affected by the genes like their parents.
Treatments There is no cure for sickle cell but there are many different treatments, including; Blood transfusions Oral antibiotics, daily. Hydroxyurea, which is an effective drug treatment for adults with severe sickle cell http://www.healthcentral.com/co mmon/images/a/A0681540_836 69_5.JPG
A Day in the Life A person diagnosed with sickle cell has to take oral antibiotics daily. This will help their immune system to fight off infections that the average body would be able to fight off on its own. Besides this, someone with sickle cell does not have to do anything different from the average person.
Resources for Those Wanting Information Sickle Cell Information www.scinfo.org ghr.nlm.nih.gov/condition=sicklecellanemia www.genome.gov/10001219 www.sicklecelldisease.org www.nichcy.org
Etc. My brother was diagnosed with sickle cell when he was born. When he gets sick it’s pretty severe, but fortunately for me and my family this is rare & he’s pretty much really healthy (: