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Presented By:-Laxmi kumari
BLOOD DISORDERS
Sickle cell anemia
Haemophilia
Anemia
Thalessemia
Leukemia
It is a genetic disorder that affects red
blood cells causing them to become
sickle shaped.
RBCs aren’t enough healthy to carry
adequate oxygen throughout body.
It is due to abnormal hemoglobin.
Discribed in 1910 by Dr. James Herrick
In 1917 – Genetic basis for SCD by Dr. V. Emmel
In 1922 - Dr. V.R Mason names the disease Sickle Cell
Anemia.
Autosomal recessive disorder.
Arise from a mutation in Hb-gene
Normally, human RBCs are flexible & round moving easily
through blood vessels. But in this case it become sickle
shaped, irregular, sticky & rigid that’s why it also sticks
with blood vessel
 If one parent has sickle
cell anemia trait
(HbAS) and the other
has sickle cell anemia
(HbSS) then there is
50% chances of any
given child will get
sickle cell anemia
 In this case, no child
will be compelety
unaffected
 If both parents have
sickle cell trait (HbAS)
then there will only
25% chances to be
child with sickle cell
anemia
 25% child will be
totally normal
 And other 50% with
sickle cell anemia trait
There are some symptoms of SCA
•Anemia
•Periodic pain
• Painful swelling of hands and feet
•Frequent infection
•Delayed growth
•Vision problem
SCA can lead to host of complications, such as:
• Organ Damage
• Leg ulcer
• Blindness
• Gallstones
• Acute chest syndrome
• Pulmonary hypertension
• stroke
 Blood test for hemoglobin s
Blood disorder

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Blood disorder

  • 4. It is a genetic disorder that affects red blood cells causing them to become sickle shaped. RBCs aren’t enough healthy to carry adequate oxygen throughout body. It is due to abnormal hemoglobin.
  • 5. Discribed in 1910 by Dr. James Herrick In 1917 – Genetic basis for SCD by Dr. V. Emmel In 1922 - Dr. V.R Mason names the disease Sickle Cell Anemia. Autosomal recessive disorder. Arise from a mutation in Hb-gene Normally, human RBCs are flexible & round moving easily through blood vessels. But in this case it become sickle shaped, irregular, sticky & rigid that’s why it also sticks with blood vessel
  • 6.
  • 7.
  • 8.  If one parent has sickle cell anemia trait (HbAS) and the other has sickle cell anemia (HbSS) then there is 50% chances of any given child will get sickle cell anemia  In this case, no child will be compelety unaffected
  • 9.  If both parents have sickle cell trait (HbAS) then there will only 25% chances to be child with sickle cell anemia  25% child will be totally normal  And other 50% with sickle cell anemia trait
  • 10.
  • 11. There are some symptoms of SCA •Anemia •Periodic pain • Painful swelling of hands and feet •Frequent infection •Delayed growth •Vision problem
  • 12. SCA can lead to host of complications, such as: • Organ Damage • Leg ulcer • Blindness • Gallstones • Acute chest syndrome • Pulmonary hypertension • stroke
  • 13.  Blood test for hemoglobin s