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https://www.um.edu.mt/library/oar/handle/123456789/82317| Title: | Hemolytic anemia due to heterozygosity for Hb C, α+-Thalassemia and hereditary xerocytosis |
| Authors: | Felice, Alex Abraham, M. Bockman, D. McKie, Virgil C. Greenberg, M. |
| Keywords: | Hemoglobin Hemoglobinopathy Sickle cell anemia Molecular microbiology |
| Issue Date: | 1987 |
| Publisher: | American Society of Hematology |
| Citation: | Felice, A., Abraham, M., Bockman, D., McKie, V. C., & Greenberg, M. (1987). Hemolytic anemia due to heterozygosity for Hb C, α+-Thalassemia and hereditary xerocytosis. Twenty-ninth Annual Meeting of the American Society of Hematology, Washington, DC. 63. |
| Abstract: | Microcytosis among Black children without significant anemia is often due to α+-thalassemia, or Hb C trait or combinations of the two. Among these we identified a 4-year-old boy with a history of pallor, intermittent icterus, and frequent hospitalization because of chest infections. |
| URI: | https://www.um.edu.mt/library/oar/handle/123456789/82317 |
| Appears in Collections: | Scholarly Works - FacM&SSur |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| Hemolytic_anemia_due_to_heterozygosity_for_Hb_C_α+-Thalassemia_and_hereditary_xerocytosis_1987.pdf | 2.08 MB | Adobe PDF | View/Open |
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