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Thalassemia
(redirected from thalassaemia major)

   Also found in: Dictionary/thesaurus, Medical, 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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Getting married should be a rational decision, knowing that your child will have thalassaemia major isn't fair for the child," said Merdas.
They said cousins marriages are the main cause of increasing cases of thalassaemia major in children which can be severely debilitating to the patient and may cause great financial and mental strain for the family.
0] thalassaemia demonstrates variable severity, ranging from a condition similar to [beta] thalassaemia minor to something approaching thalassaemia major.
 
 
 
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