Probable transfusion transmitted malaria in child of sickle cell disease (HbSS)
โ Scribed by Sameer Agarwal; Swati Maini; Arundhati A. Kelkar; Jayshree R. Tijare; A. V. Shrikhande
- Book ID
- 107598288
- Publisher
- Springer-Verlag
- Year
- 2008
- Tongue
- English
- Weight
- 97 KB
- Volume
- 75
- Category
- Article
- ISSN
- 0019-5456
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๐ SIMILAR VOLUMES
The treatment of various complications of sickle cell disease has included red cell exchange in the past, and the development of automated pheresis equipment has greatly simplified such exchanges. Traditionally, the patient's red cells have been exchanged while their plasma was returned to them. Rec
## Abstract Patients with sickle cell disease (SCD) appear to be at lower risk of endocrinopathies and cardiac dysfunction than those with thalassemia major (TM). Circulating redox active iron is lower in these patients, possibly due to increased systemic inflammation and circulating cytokines. Hep