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Fanconi aplastic anemia associated with β-thalassemia trait

✍ Scribed by Altay, Cigdem; Gürgey, Aytemiz; Basak, A. Nazli; Tadmouri, Ghazi O.; Schroeder-Kurt, T.

Publisher
John Wiley and Sons
Year
1996
Tongue
English
Weight
236 KB
Volume
52
Category
Article
ISSN
0361-8609

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A 14-month-old boy was referred to our hospital for evaluation of severe anemia. In the bone marrow aspiration smear, normal cellularity with severe erythroblastopenia (3%) was observed. The hemoglobin electrophoresis of the patient and his father were compatible with the b-thalassemia trait. Becaus