Sickle-β+ thalassemia with splenic calcification and bone marrow infarction: a case report

Author:

Kar Rakhee,Das Reena,Saxena Akshay,Chawla Y.,Ahluwalia Jasmina

Publisher

Springer Science and Business Media LLC

Subject

Hematology

Reference14 articles.

1. Steinberg MH (2001) Compound heterozygous and other sickle hemoglobinopathies. In: Disorders of hemoglobin: genetics, Pathophysiology and clinical management. Edn. Cambridge University Press, pp 786

2. Wang WC Sickle cell anemia and other sickling syndromes. In: Wintrobe’s clinical hematology, 11th edn. Lippincott Williams and Wilkins, pp 1295

3. Silverstroni E, Bianco I (1946) Una nova entita noso logica: La malatia micro drepanocitica. Hematologica 29:455

4. Li J, Plonczynski M, Kheradpour A, et al (1998) Severe HbS-β+ thalassemia caused by IVS-1 splice site mutations. Hemoglobin 22:383–385

5. Poillon WN, Kim BC, Rodgers GP, et al (1993) Sparing effect of hemoglobin F and Hemoglobin A2 on polymerization of hemoglobin S at physiological ligand saturations. Proc Natl Acad Sci 90:5039–5043

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