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Sickle Cell Anemia

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Sickle Cell Anemia Murron Qualls Biology 6th Names of Sickle Cell Anemia SCD SCA Hemoglobin SS disease (Hb SS) Who is most likely to get SCA? People of African and ... – PowerPoint PPT presentation

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Title: Sickle Cell Anemia


1
Sickle Cell Anemia
  • Murron Qualls
  • Biology 6th

2
Names of Sickle Cell Anemia
  • SCD
  • SCA
  • Hemoglobin SS disease (Hb SS)

3
Who is most likely to get SCA?
  • People of African and Mediterranean are the most
    common to get the disease.
  • People from South and Central America, the
    Caribbean, and the Middle East are also more
    likely to get it then most.

4
Symptoms
  • Common symptoms include
  • Abdominal pain
  • Bone pain
  • Breathlessness
  • Delayed growth and puberty
  • Fatigue
  • Fever
  • Jaundice
  • Paleness
  • Rapid heart rate
  • Ulcers on the lower legs (in children and adults)
  • Other symptoms include
  • Chest pain
  • Excessive thirst
  • Frequent urination
  • Painful and prolonged erection
  • Poor eyesight and sometimes blindness
  • Skin ulcers
  • Strokes

5
How common is this disease?
  • About 70,000 people currently have SCD in the
    United States
  • About 1 in 12 African Americans has sickle cell
    trait
  • The disease occurs in about 1 out of every 500
    African Americans births. 
  • The disease occurs in about 1 out of every 36,000
    Hispanic Americans births.

6
Is the Disease Deadly?
  • Sickle cell anemia is deadly but not always
  • Most people who die from this disease die between
    the age of 20 and 40 of organ failure
  • Now, people can live into their fifty's if caught
    early and treated right.

7
Can You be Tested?
  • Yes, you can be testes for sickle cell anemia.
  • The diagnosis can be made as early as pregnancy
  • Some tests that can be done
  • Complete blood count (CBC)
  • Hemoglobin electrophoresis
  • Sickle cell test
  • Blood oxygen
  • Serum potassium

8
Is there Treatment?
  • There is treatment
  • Treatment is for life
  • Treatment includes pain killers
  • Treatment includes folic acid which helps make
    red blood cells
  • Treatment does not cure SCD
  • Other Treatments
  • Dialysis or kidney transplant for kidney disease
  • Gallbladder removal (if you have gallstone
    disease)
  • Hip replacement for avascular necrosis of the hip
  • Wound care, zinc oxide, or surgery for leg ulcers

9
Are there Support Groups?
  • There are many support groups all across America
    at hospitals, cancer treatment places and small
    organizations
  • There are many online support groups

Sickle Cell Parent Group Chicago, Illinois
10
Interesting Facts
  • Some people only have attacks every few years
    while some have many a day
  • Sickle cell anemia is found in one of every
    twelve African Americans
  • People with SCA should not go on planes because
    the air pressure can cause them to stop breathing

11
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