Abstract
The management of Beta Thalassemia, the commonest form of hemolytic anemia in children, has changed significantly in the last few years. With the availability of better transfusion regimen, iron chelation therapy, proper management of complications and good supportive care, it is now possible for a thalassemic child to have a near normal life span with a good quality of life.
MeSH terms
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Adaptation, Psychological
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Bacterial Infections / epidemiology
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Cardiovascular Diseases / epidemiology
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Chelation Therapy
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Child
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Comorbidity
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Diabetes Mellitus / epidemiology
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Fertility
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Growth Disorders / epidemiology
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Humans
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Hypoparathyroidism / epidemiology
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Hypothyroidism / epidemiology
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Iron Overload / epidemiology
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Iron Overload / etiology
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Transfusion Reaction
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beta-Thalassemia / epidemiology
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beta-Thalassemia / physiopathology
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beta-Thalassemia / therapy*