STUDY OF MORBIDITY PATTERN IN CHILDREN WITH TRANSFUSION DEPENDENT THALASSEMIA
Heba Tallah Ahmed Ali Elawa;
Abstract
eta-thalassaemia represents a group of recessively inherited haemoglobin disorders characterized by deficient synthesis of the b globin chain. The homozygous state results in severe anaemia in infancy which requires regular blood transfusion.
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Other data
| Title | STUDY OF MORBIDITY PATTERN IN CHILDREN WITH TRANSFUSION DEPENDENT THALASSEMIA | Other Titles | دراسة معدل الأصابة بالمضاعفات فى الأطفال المصابين بمرض انيميا البحر المتوسط | Authors | Heba Tallah Ahmed Ali Elawa | Keywords | STUDY OF MORBIDITY PATTERN IN CHILDREN WITH TRANSFUSION DEPENDENT THALASSEMIA | Issue Date | 2011 | Description | eta-thalassaemia represents a group of recessively inherited haemoglobin disorders characterized by deficient synthesis of the b globin chain. The homozygous state results in severe anaemia in infancy which requires regular blood transfusion. The most |
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| 107016p4391.pdf | 769.69 kB | Adobe PDF | View/Open |
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