A 78-year-old man with sickle-cell anemia
β Scribed by Koduri, Prasad Rao; Leon, Monica; Honig, George R.; Lu, Shi-Jiang
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 49 KB
- Volume
- 62
- Category
- Article
- ISSN
- 0361-8609
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## Abstract The diseases commonly confused with sickle cell anemia include sickle cellΞ²βthalassemia in which synthesis of Ξ²^A^βchains are completely suppressed (HbSβΞ²^O^βthalassemia). We obtained hematologic measurements and studied globin biosynthesis in five patients with this disorder and compar
CLINICOPATHOLOGIC CONFERENCE 1358 \* N/A Ο not applicable; SGOT Ο serum glutamic oxaloacetic transaminase; SGPT Ο serum glutamic pyruvic transaminase; hpf Ο high-power field; ANA Ο antinuclear antibodies; ESR Ο erythrocyte sedimentation rate; ANCA Ο antineutrophil cytoplasmic antibody.