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Sickle Cell 
Anemia 
Sample Project 
Biology – Mr. Woolf 
Image source: 9
What is sickle cell? 
• Sickle cell disease (SCD) affects the 
production of red blood cells in the 
body. Hemoglobin, the protein in blood 
cells that carries oxygen, is not produced 
correctly. This gives affected blood cells 
a sickle, or crescent, shape. These blood 
cells tend to be stiff and sticky, and they 
can block blood vessels in limbs and 
organs. This can cause pain, organ 
damage, and increased risk of 
infections.13 The structure of hemoglobin 15
What is sickle cell? 
• Sickle cell anemia is one common form 
of sickle cell disease. Anemia is a 
condition in which the body does not 
have enough red blood cells. Sickle cell 
anemia occurs because sickle cells die 
more quickly than normal blood cells, 
and the body’s bone marrow cannot 
replace the blood cells quickly enough.13 
• Sickle cell anemia can lead to many 
complications, including stroke, high 
blood pressure, blindness, skin ulcers, 
gallstones, and a life-threatening 
condition called acute chest syndrome. 8 
Image source: 13
How common is sickle cell? 
• Sickle cell is most common among populations with ancestry in 
sub-Saharan Africa; Spanish-speaking regions in the Western 
Hemisphere (South America, the Caribbean, and Central America); 
Saudi Arabia; India; and Mediterranean countries such as Turkey, 
Greece, and Italy. The CDC estimates that in the U.S.: 
• SCD affects 90,000 to 100,000 Americans. 
• SCD occurs among about 1 out of every 500 Black or African-American 
births. 
• SCD occurs among about 1 out of every 36,000 Hispanic-American 
births. 
• About 1 in 12 African Americans carries the gene for the sickle cell 
trait. 2
What causes sickle cell? 
• Sickle cell is caused by a mutation in the hemoglobin, 
beta gene, referred to as the HBB gene. This gene is 
located on the short arm of Chromosome 11, and it 
controls the production of the protein hemoglobin. 
• The HBB gene contains 1,605 nucleotide base pairs, and 
the hemoglobin gene is a sequence of 535 amino acids. 
• A change in one nucleotide causes 
a single amino acid in the protein to 
change: glutamic acid is replaced 
with lysine. This causes the sickle 
cell trait.5
What causes sickle cell? 
• The sickle cell gene is considered an autosomal recessive 
trait. A person must inherit the sickle cell gene from both 
parents in order to exhibit the disease. 
• If a person only inherits s copy of the gene from one 
parent, that person is considered a carrier – this person 
would be said to have the sickle cell trait (SCT), but not 
sickle cell disease (SCD). Carriers do not exhibit 
symptoms of the disease.16 
Image source: 10
What causes sickle cell? 
Image source: 11
Diagnosing sickle cell 
• Sickle cell disease and the presence of the sickle cell trait can 
be diagnosed with blood tests or genetic tests. 
• Sickle cell can be diagnosed at any age, but testing of 
newborns is preferred, so that treatment can start as early as 
possible. 
• The disease can be diagnosed before birth by testing amniotic 
fluid or placental tissue. 
• Parents can be tested for the trait using the same blood tests in 
order to determine if they are carriers. 
(http://www.chop.edu/service/hematology/our-programs/ 
sickle-cell-center/diagnosing-and-treating-sickle-cell- 
disease.html#when_best)
Treatment of sickle cell 
• In the past, people with sickle cell disease often died 
between ages 20 and 40. With treatment, people now live 
to the age of 50 and beyond.16 
• A bone marrow transplant (a.k.a, stem cell translpant) can 
potentially cure children will sickle cell with success rates 
of approximately 85% . However, a donor must be 
available, and the transplant procedure is risky, resulting 
fatality in 5-10% of cases. Therefore, it is typically only 
used in severe cases.6 
Image source: 7
Treatment of sickle cell 
• Ongoing treatments for the symptoms of SCD include 
drugs (pain relievers, antibiotics, hydroxyuria), blood 
transfusions to reduce stroke risks, vaccines to reduce 
infection risk, and supplemental oxygen. 
• During 2005, medical expenditures for children with 
SCD averaged $11,702 for children with Medicaid 
coverage and $14,772 for children with employer-sponsored 
insurance. About 40% of both groups had at 
least one hospital stay. 2
Interesting fact… 
• People who carry the sickle cell trait are resistant to 
malaria, a deadly insect-born disease. Many researchers 
believe that this survival advantage accounts for high 
rates of the sickle cell trait in populations that descend 
from areas where malaria was historically common.10
Global malaria vectors 
Image source: 4
Families and sickle cell 
Tiffany Dews, 33 
Richmond, Va. 
“When I first got pregnant, my intention was not to be a stay-at-home mom. 
My intention was to work and finish school, but of course, plans change. 
Both my husband and I have the trait for sickle cell disease, and combined 
we have two children, Tracy and Riley, with the disease. There’s a one in 
four chance each time we decide to have kids that we would pass on the 
disease. 
Years ago, [children with sickle cell disease] were not making it past the age 
of 20 or 21. So my hope is that they will have kids, and hopefully not have 
kids with the disease.” 1
Families and sickle cell 
• For a family with insurance, typical medical costs for a family 
member with sickle cell disease range from $10,000-15,000 per 
year.2 
• Parents of children with sickle cell disease need to educate 
themselves about symptoms and complications of the disease, and 
must monitor their child carefully. Children with the disease will 
require frequent doctor’s visits.12 
• Patients and family members often benefit from support groups, 
where they can share information and coping strategies.12 
• A person with a family history of sickle cell may want to be tested for 
the trait, and may consider this information when making 
reproductive and family planning decisions.12
References 
1. Barrow, K. (2011, March 07). Pain, persistence, family: Sickle cell disease. Retrieved April 15, 2014, from 
http://www.nytimes.com/2011/03/08/health/views/08sickle.html?_r=0 
2. Center for Disease Control and Prevention. (n.d.). Sickle cell data and statistics. Retrieved April 15, 2014, 
from http://www.cdc.gov/ncbddd/sicklecell/data.html 
3. Children's Hosoital of Philadelphia. (n.d.). Overview of sickle cell disease. Retrieved April 15, 2014, from 
http://www.chop.edu/service/hematology/our-programs/sickle-cell-center/diagnosing-and-treating-sickle- 
cell-disease.html#when_best 
4. Despommier, D., Racaniello, V., & White, J. (2004). Malaria. Retrieved October 20, 2014, from 
http://www.medicalecology.org/diseases/malaria/malaria.htm. 
5. Genetics Home Reference staff, National Institutes of Health. (2009). HBB. Retrieved April 15, 2014, 
from http://ghr.nlm.nih.gov/gene/HBB 
6. Healthwise staff. (2014, March 12). Stem cell transplant for sickle cell disease. Retrieved April 15, 2014, 
from http://www.webmd.com/cancer/bone-marrow-transplant-for-sickle-cell-disease 
7. Leukemia: Improving efficiency of bone marrow transplants. (n.d.). Retrieved April 15, 2014, from 
http://fbresearch.org/leukemia-improving-efficiency-of-bone-marrow-transplants/ 
8. Mayo Clinic. (n.d.). Sickle cell anemia - complications. Retrieved April 15, 2014, from 
http://www.mayoclinic.org/diseases-conditions/sickle-cell-anemia/basics/complications/con- 
20019348 
9. NHS England. (2014, May 21). Sickle cell anaemia: Causes. Retrieved April 15, 2014, from 
http://www.nhs.uk/Conditions/Sickle-cell-anaemia/Pages/Causes.aspx
References (cont.) 
10. Mutations and malaria: Pauling's adventure in genetics. (2009, January 13). Retrieved April 15, 2014, from 
http://paulingblog.wordpress.com/2009/01/13/mutations-and-malaria-paulings-adventure-in-genetics 
11. Miller-Keane Encyclopedia and Dictionary of Medicine, Nursing, and Allied Health, Seventh Edition. 
(2003). Retrieved April 15, 2014, from http://medical-dictionary. 
thefreedictionary.com/sickle%2Bcell%2Bdisease 
12. National Institutes of Health. (2012, September 28). Living with sickle cell anemia. Retrieved April 15, 
2014, from http://www.nhlbi.nih.gov/health/health-topics/topics/sca/livingwith.html 
13. National Institutes of Health. (2012, September 28). What is sickle cell anemia? Retrieved April 15, 2014, 
from http://www.nhlbi.nih.gov/health/health-topics/topics/sca 
14. Oregon State University Libraries Special Collections & Research Center. (2009, January 13). Mutations 
and malaria: Pauling's adventure in genetics. Retrieved April 15, 2014, from 
http://paulingblog.wordpress.com/2009/01/13/mutations-and-malaria-paulings-adventure-in-genetics 
15. Reproduced pastel drawing of the hemoglobin structure. (n.d.). Retrieved April 15, 2014, from 
http://scarc.library.oregonstate.edu/coll/pauling/blood/pictures/1964b4.1-hbmodel.html 
16. U.S. National Libraries of Medicine, National Institutes of Health. (2014, February 24). Sickle cell 
anemia. Retrieved April 15, 2014, from 
http://www.nlm.nih.gov/medlineplus/ency/article/000527.htm

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Sickle cell anemia

  • 1. Sickle Cell Anemia Sample Project Biology – Mr. Woolf Image source: 9
  • 2. What is sickle cell? • Sickle cell disease (SCD) affects the production of red blood cells in the body. Hemoglobin, the protein in blood cells that carries oxygen, is not produced correctly. This gives affected blood cells a sickle, or crescent, shape. These blood cells tend to be stiff and sticky, and they can block blood vessels in limbs and organs. This can cause pain, organ damage, and increased risk of infections.13 The structure of hemoglobin 15
  • 3. What is sickle cell? • Sickle cell anemia is one common form of sickle cell disease. Anemia is a condition in which the body does not have enough red blood cells. Sickle cell anemia occurs because sickle cells die more quickly than normal blood cells, and the body’s bone marrow cannot replace the blood cells quickly enough.13 • Sickle cell anemia can lead to many complications, including stroke, high blood pressure, blindness, skin ulcers, gallstones, and a life-threatening condition called acute chest syndrome. 8 Image source: 13
  • 4. How common is sickle cell? • Sickle cell is most common among populations with ancestry in sub-Saharan Africa; Spanish-speaking regions in the Western Hemisphere (South America, the Caribbean, and Central America); Saudi Arabia; India; and Mediterranean countries such as Turkey, Greece, and Italy. The CDC estimates that in the U.S.: • SCD affects 90,000 to 100,000 Americans. • SCD occurs among about 1 out of every 500 Black or African-American births. • SCD occurs among about 1 out of every 36,000 Hispanic-American births. • About 1 in 12 African Americans carries the gene for the sickle cell trait. 2
  • 5. What causes sickle cell? • Sickle cell is caused by a mutation in the hemoglobin, beta gene, referred to as the HBB gene. This gene is located on the short arm of Chromosome 11, and it controls the production of the protein hemoglobin. • The HBB gene contains 1,605 nucleotide base pairs, and the hemoglobin gene is a sequence of 535 amino acids. • A change in one nucleotide causes a single amino acid in the protein to change: glutamic acid is replaced with lysine. This causes the sickle cell trait.5
  • 6. What causes sickle cell? • The sickle cell gene is considered an autosomal recessive trait. A person must inherit the sickle cell gene from both parents in order to exhibit the disease. • If a person only inherits s copy of the gene from one parent, that person is considered a carrier – this person would be said to have the sickle cell trait (SCT), but not sickle cell disease (SCD). Carriers do not exhibit symptoms of the disease.16 Image source: 10
  • 7. What causes sickle cell? Image source: 11
  • 8. Diagnosing sickle cell • Sickle cell disease and the presence of the sickle cell trait can be diagnosed with blood tests or genetic tests. • Sickle cell can be diagnosed at any age, but testing of newborns is preferred, so that treatment can start as early as possible. • The disease can be diagnosed before birth by testing amniotic fluid or placental tissue. • Parents can be tested for the trait using the same blood tests in order to determine if they are carriers. (http://www.chop.edu/service/hematology/our-programs/ sickle-cell-center/diagnosing-and-treating-sickle-cell- disease.html#when_best)
  • 9. Treatment of sickle cell • In the past, people with sickle cell disease often died between ages 20 and 40. With treatment, people now live to the age of 50 and beyond.16 • A bone marrow transplant (a.k.a, stem cell translpant) can potentially cure children will sickle cell with success rates of approximately 85% . However, a donor must be available, and the transplant procedure is risky, resulting fatality in 5-10% of cases. Therefore, it is typically only used in severe cases.6 Image source: 7
  • 10. Treatment of sickle cell • Ongoing treatments for the symptoms of SCD include drugs (pain relievers, antibiotics, hydroxyuria), blood transfusions to reduce stroke risks, vaccines to reduce infection risk, and supplemental oxygen. • During 2005, medical expenditures for children with SCD averaged $11,702 for children with Medicaid coverage and $14,772 for children with employer-sponsored insurance. About 40% of both groups had at least one hospital stay. 2
  • 11. Interesting fact… • People who carry the sickle cell trait are resistant to malaria, a deadly insect-born disease. Many researchers believe that this survival advantage accounts for high rates of the sickle cell trait in populations that descend from areas where malaria was historically common.10
  • 12. Global malaria vectors Image source: 4
  • 13. Families and sickle cell Tiffany Dews, 33 Richmond, Va. “When I first got pregnant, my intention was not to be a stay-at-home mom. My intention was to work and finish school, but of course, plans change. Both my husband and I have the trait for sickle cell disease, and combined we have two children, Tracy and Riley, with the disease. There’s a one in four chance each time we decide to have kids that we would pass on the disease. Years ago, [children with sickle cell disease] were not making it past the age of 20 or 21. So my hope is that they will have kids, and hopefully not have kids with the disease.” 1
  • 14. Families and sickle cell • For a family with insurance, typical medical costs for a family member with sickle cell disease range from $10,000-15,000 per year.2 • Parents of children with sickle cell disease need to educate themselves about symptoms and complications of the disease, and must monitor their child carefully. Children with the disease will require frequent doctor’s visits.12 • Patients and family members often benefit from support groups, where they can share information and coping strategies.12 • A person with a family history of sickle cell may want to be tested for the trait, and may consider this information when making reproductive and family planning decisions.12
  • 15. References 1. Barrow, K. (2011, March 07). Pain, persistence, family: Sickle cell disease. Retrieved April 15, 2014, from http://www.nytimes.com/2011/03/08/health/views/08sickle.html?_r=0 2. Center for Disease Control and Prevention. (n.d.). Sickle cell data and statistics. Retrieved April 15, 2014, from http://www.cdc.gov/ncbddd/sicklecell/data.html 3. Children's Hosoital of Philadelphia. (n.d.). Overview of sickle cell disease. Retrieved April 15, 2014, from http://www.chop.edu/service/hematology/our-programs/sickle-cell-center/diagnosing-and-treating-sickle- cell-disease.html#when_best 4. Despommier, D., Racaniello, V., & White, J. (2004). Malaria. Retrieved October 20, 2014, from http://www.medicalecology.org/diseases/malaria/malaria.htm. 5. Genetics Home Reference staff, National Institutes of Health. (2009). HBB. Retrieved April 15, 2014, from http://ghr.nlm.nih.gov/gene/HBB 6. Healthwise staff. (2014, March 12). Stem cell transplant for sickle cell disease. Retrieved April 15, 2014, from http://www.webmd.com/cancer/bone-marrow-transplant-for-sickle-cell-disease 7. Leukemia: Improving efficiency of bone marrow transplants. (n.d.). Retrieved April 15, 2014, from http://fbresearch.org/leukemia-improving-efficiency-of-bone-marrow-transplants/ 8. Mayo Clinic. (n.d.). Sickle cell anemia - complications. Retrieved April 15, 2014, from http://www.mayoclinic.org/diseases-conditions/sickle-cell-anemia/basics/complications/con- 20019348 9. NHS England. (2014, May 21). Sickle cell anaemia: Causes. Retrieved April 15, 2014, from http://www.nhs.uk/Conditions/Sickle-cell-anaemia/Pages/Causes.aspx
  • 16. References (cont.) 10. Mutations and malaria: Pauling's adventure in genetics. (2009, January 13). Retrieved April 15, 2014, from http://paulingblog.wordpress.com/2009/01/13/mutations-and-malaria-paulings-adventure-in-genetics 11. Miller-Keane Encyclopedia and Dictionary of Medicine, Nursing, and Allied Health, Seventh Edition. (2003). Retrieved April 15, 2014, from http://medical-dictionary. thefreedictionary.com/sickle%2Bcell%2Bdisease 12. National Institutes of Health. (2012, September 28). Living with sickle cell anemia. Retrieved April 15, 2014, from http://www.nhlbi.nih.gov/health/health-topics/topics/sca/livingwith.html 13. National Institutes of Health. (2012, September 28). What is sickle cell anemia? Retrieved April 15, 2014, from http://www.nhlbi.nih.gov/health/health-topics/topics/sca 14. Oregon State University Libraries Special Collections & Research Center. (2009, January 13). Mutations and malaria: Pauling's adventure in genetics. Retrieved April 15, 2014, from http://paulingblog.wordpress.com/2009/01/13/mutations-and-malaria-paulings-adventure-in-genetics 15. Reproduced pastel drawing of the hemoglobin structure. (n.d.). Retrieved April 15, 2014, from http://scarc.library.oregonstate.edu/coll/pauling/blood/pictures/1964b4.1-hbmodel.html 16. U.S. National Libraries of Medicine, National Institutes of Health. (2014, February 24). Sickle cell anemia. Retrieved April 15, 2014, from http://www.nlm.nih.gov/medlineplus/ency/article/000527.htm