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Did you Know? Did You Know
To improve patient compliance with chelation therapy, researches are at work on new chelators that require less frquent and prolonged infusions or may be taken orally.

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Thalassemia

Thalassemia is an inherited characteristic of the blood. It reduces the amount of hemoglobin in a human body, leading to anemia.
Deficiency or a lesser count of red blood cells, or too little hemoglobin in blood, is Anemia - which simply means a shortage of blood.
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Treatment

Blood Transfusion is one of the most regularly practiced treatments for Thalassemia. To be precise, the treatment is not blood transfusion, but transfusion of red blood cells. These transfusions are necessary to provide the patient with a temporary supply of healthy red blood cells..
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Events, Updates, New Studies!

1) thalpal.com re-direct

2) How to post new and reply to t...

3) 2. PanEuropean conference

4) Free Screening!

5) 6th National Thalassaemia Conf...

6) Iron Warriors Art Contest

7) Aga Khan - Celebrating 100 Bon...

8) 4th International Conference o...

9) 2009 TAG Conference October 21...

10) Participants Needed for Survey...

11) Notes from the Egyptian and Sy...

12) 3rd TSF Conference, North Holl...

13) EUMEDCONNECT2 video on thalass...

14) New Book about Thalassemia (Co...

15) New Thalpal Group on Facebook

16) Share your opinion on Clinical...

17) husaini thalassaemia day

18) world thalassaemia day

19) 1st Pan-Middle Eastern Confere...

20) International Thal Conference ...

Research Material

Most Read   Chapter 1: What Happens in Thalassemia Major? (9530 Times)
Most Sent   Section IV: Thalassemia Associated With an Abnormal Hemoglobin (7 Times)
Most Bookmarked   Chapter 1: What Happens in Thalassemia Major? (30 Times)

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