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M.R COLLEGE OF EDUCATION.
NAME OF UNIVERSITY: W.B.U.T.T.E.P.A
NAME OF STUDENT: PINKI SAHA
COLLEGE ROLL NO: 10
University Roll : 150152 No. : 17034
COURSE : EPC 3
TOPIC: THALASSEMIA
COURSE V (1.1.5)
TOPIC: THALASSEMIA
What is thalassemia?
• Thalassemia is an inherited blood disorder.
• The protein hemoglobin transports oxygen around the body in
blood cells. Bone marrowuses the iron we get from food to make
hemoglobin.
• In people with thalassemia, the bone marrow does not produce
enough healthy hemoglobin or red blood cells. In some types this
leads to a lack of oxygen, resulting in anemia and fatigue.
• There are different types of thalassemia. More severe types can
involve organ damage, restricted growth, heart failure, liver
damage, and even death.
• People with mild thalassemia may not require any treatment, but
more severe forms will necessitate regular blood transfusions.
Types of Thalassemia:
1. Alpha Thalassemia:
.One faulty gene: No symptoms. Child is carrier.
.Two faulty gene: Mild Anemia..Minor thalassemia.
.Three faulty gene: Heamoglobin H disease.cronic anemia
.Four faulty gene: Major thalassemia.. Hydrops fetalis.
2. Beta Thalassemia:
. One faulty gene: Minor thalassemia
.Two faulty gene: Major thalassemia..called Colley’s
anemia
Alpha & Beta Thalassemia
Affected Organs
• Pituitary Glands
• Adrenal Glands
• Liver
• Testis
• Thyroid Glands
• Heart
• Pancreus
• Overy
SYMPTOMS OF THALESSEMIA
• Jaundice and pale skin
• Drowsiness and fatigue
• Enlarge spleen
• Iron overload
• Bone deformaties
• Poor feeding
• Delayed growth
• Rapid heart beat
TREATMENT OF THALASSEMIA
• Blood transfussion
• Iron chelation
• Bone marrow transplant
• Surgery
• Gene therapy
HERIDITY OF THALASSEMIA
Conclusion
Thalassemia is an inherited blood disorder in
which the body makes abnormal form of
heamoglobin which leads to anemia..
Prevension:
Pre marital screening to make sure that the
couple are not both carriers..
Reduction of marriages between relatives..
Reference
• Books:
1. Satra Sam Sanatan,Bosu Debasish,(january
2016),”Madhyamik Jibonbigyan o
Poribesh”,Prantik,Kolkata-700009
• Website:
www.shutterstock.com
www.wikipedia.org
 UPLOADED ADDRESS:
http://www.slideshare.net/PINKISAHA1
E content

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E content

  • 1. M.R COLLEGE OF EDUCATION. NAME OF UNIVERSITY: W.B.U.T.T.E.P.A NAME OF STUDENT: PINKI SAHA COLLEGE ROLL NO: 10 University Roll : 150152 No. : 17034 COURSE : EPC 3 TOPIC: THALASSEMIA
  • 3. What is thalassemia? • Thalassemia is an inherited blood disorder. • The protein hemoglobin transports oxygen around the body in blood cells. Bone marrowuses the iron we get from food to make hemoglobin. • In people with thalassemia, the bone marrow does not produce enough healthy hemoglobin or red blood cells. In some types this leads to a lack of oxygen, resulting in anemia and fatigue. • There are different types of thalassemia. More severe types can involve organ damage, restricted growth, heart failure, liver damage, and even death. • People with mild thalassemia may not require any treatment, but more severe forms will necessitate regular blood transfusions.
  • 4. Types of Thalassemia: 1. Alpha Thalassemia: .One faulty gene: No symptoms. Child is carrier. .Two faulty gene: Mild Anemia..Minor thalassemia. .Three faulty gene: Heamoglobin H disease.cronic anemia .Four faulty gene: Major thalassemia.. Hydrops fetalis. 2. Beta Thalassemia: . One faulty gene: Minor thalassemia .Two faulty gene: Major thalassemia..called Colley’s anemia
  • 5. Alpha & Beta Thalassemia
  • 6. Affected Organs • Pituitary Glands • Adrenal Glands • Liver • Testis • Thyroid Glands • Heart • Pancreus • Overy
  • 7. SYMPTOMS OF THALESSEMIA • Jaundice and pale skin • Drowsiness and fatigue • Enlarge spleen • Iron overload • Bone deformaties • Poor feeding • Delayed growth • Rapid heart beat
  • 8. TREATMENT OF THALASSEMIA • Blood transfussion • Iron chelation • Bone marrow transplant • Surgery • Gene therapy
  • 10. Conclusion Thalassemia is an inherited blood disorder in which the body makes abnormal form of heamoglobin which leads to anemia.. Prevension: Pre marital screening to make sure that the couple are not both carriers.. Reduction of marriages between relatives..
  • 11. Reference • Books: 1. Satra Sam Sanatan,Bosu Debasish,(january 2016),”Madhyamik Jibonbigyan o Poribesh”,Prantik,Kolkata-700009 • Website: www.shutterstock.com www.wikipedia.org  UPLOADED ADDRESS: http://www.slideshare.net/PINKISAHA1