Severe Microcytosis in a Hemoglobin E/B-Thalassemia Patient with Signs of Iron Deficiency: A Case Report
Background: β-thalassemia is a hereditary disorder characterized by a decrease in the synthesis of β-globin chains that decreases hemoglobin in erythrocytes, low erythrocyte production, and anemia. Case presentation: A 6-year-old girl came with complaints of paleness for one week. Physical examina...
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| Main Authors: | , |
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| Format: | Article PeerReviewed |
| Language: | English English English |
| Published: |
Elsevier BV
2022
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| Subjects: | |
| Online Access: | https://repository.unair.ac.id/127479/1/jurnal%20INTER-1.pdf https://repository.unair.ac.id/127479/2/Karil-INTER-1.pdf https://repository.unair.ac.id/127479/3/Turnitin-INTER-1.pdf https://repository.unair.ac.id/127479/ |
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| Institution: | Universitas Airlangga |
| Language: | English English English |