Multiorgan failure during a sickle cell crisis in sickle/β+-thalassemia
✍ Scribed by Fasika M Tedla; Eli A Friedman
- Book ID
- 114204086
- Publisher
- Elsevier Science
- Year
- 2003
- Tongue
- English
- Weight
- 65 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0272-6386
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We have analyzed the hemoglobin abnormalities in nearly 50 Albanian patients with a significant hemoglobinopathy and included 37 relatives in this study. Sickle cell anemia (SS) is a common disorder; all 15 sickle cell anemia patients had the complications expected for this disease. The beta S haplo
## Abstract The diseases commonly confused with sickle cell anemia include sickle cellβ‐thalassemia in which synthesis of β^A^‐chains are completely suppressed (HbS‐β^O^‐thalassemia). We obtained hematologic measurements and studied globin biosynthesis in five patients with this disorder and compar