PO85 | Acute retinal ischemia in hemoglobin SC disease: a case report and review of the literature
Background: Sickle cell disease (SCD) encompasses a group of hereditary hemoglobinopathies characterized by the presence of hemoglobin S (HbS), and includes homozygous sickle cell anemia (HbSS), sickle β⁰-thalassemia (HbS/β⁰), and heterozygous disorders, such as HbSC disease. The latter results fro...
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| Format: | Article |
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| Language: | English |
| Published: |
PAGEPress Publications
2025-08-01
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| Series: | Bleeding, Thrombosis and Vascular Biology |
| Subjects: | |
| Online Access: | https://www.btvb.org/btvb/article/view/354 |
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