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Splenic sequestration crisis as an index manifestation of heterozygous hemoglobinopathy in an adult
Sickle β(+)-thalassemia rarely manifests with acute splenic sequestration crisis in adults. We report a case of a 20-year-old female who presented with fever and left upper quadrant abdominal pain. Laboratory studies revealed hemolytic anemia. Tests for autoimmune hemolysis and hemolytic diseases we...
Kaydedildi:
| Yayımlandı: | Oxf Med Case Reports |
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| Asıl Yazarlar: | , , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Oxford University Press
2019
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6624996/ https://ncbi.nlm.nih.gov/pubmed/31312463 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/omcr/omz069 |
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