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Thalassemia
(redirected from thalassemia major)

   Also found in: Dictionary/thesaurus, Medical, Legal, Wikipedia 0.01 sec.
thalassemia [‚thal·ə′sē·mē·ə]
(medicine)
A hereditary form of hemolytic anemia resulting from a defective synthesis of hemoglobin: thalassemia major is the homozygous state accompanied by clinical illness, and thalassemia minor is the heterozygous state and may not have evident clinical manifestations. Also known as Mediterranean anemia.

Thalassemia 

(also thalassanemia), a familial hemolytic anemia, first detected in 1925 among inhabitants of the Mediterranean region. Thalassemia is caused by disturbances in hemoglobin synthesis.



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5 lakh Thalassemia Major Patients in Pakistan as compared to mere 1000 patients in UK and approximately 10% of Pakistans population is estimated to have Thalassemia traits (Thalassemia Minor) thus over 1.
The thalassemia-minor conditions produce minimal decrements in the Hb concentration; whereas, thalassemia intermedia and thalassemia major may be associated with moderate to severe decreases in Hb concentration.
At that point in time, we found out that Hussain was suffering from both scoliosis and Thalassemia major (a severe form of anaemia and oxygen depletion) which requires 280 milligrams of blood replacement every three weeks," said his father, Alaa Abdul Kareem.
 
 
 
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