Social Impact and Quality of Life of Patients with β-Thalassaemia: A Systematic Review
β-Thalassaemia (BT) is a hereditary genetic blood disease caused by a mutation in the gene that encodes the haemoglobin protein. In the most severe forms, BT forces patients to undergo frequent blood transfusions, which has a significant impact on the quality of life. Classified as rare, BT is very...
| Main Authors: | , |
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| Format: | Article |
| Language: | English |
| Published: |
European Medical Journal
2022-04-01
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| Series: | European Medical Journal Hematology |
| Online Access: | https://www.emjreviews.com/hematology/article/social-impact-and-quality-of-life-of-patients-with-%ce%b2-thalassaemia-a-systematic-review/ |