Sickle cell disease: a comparative perspective on global and national initiatives
Sickle cell disease (SCD) is a genetic disorder caused by mutations in the β-globin chain of hemoglobin, leading to abnormal red blood cells, severe pain, anemia, organ damage, and increased infection risk. Inherited in an autosomal recessive manner, it mainly affects regions with high malaria incid...
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| Hlavní autoři: | , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
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Frontiers Media S.A.
2024-08-01
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| Edice: | Frontiers in Hematology |
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| On-line přístup: | https://www.frontiersin.org/articles/10.3389/frhem.2024.1457158/full |
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