Peripheral Blood Smear Findings in 2 Patients With Coexisting Thalassemia and Hereditary Spherocytosis
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Oncology,Hematology,Pediatrics, Perinatology and Child Health
Reference6 articles.
1. Hereditary spherocytosis overlooked for 7 years in a pediatric patient with β-thalassemia trait and novel compound heterozygous mutations of SPTA1 gene;Chen;Hematology,2020
2. α-thalassemia combined with hereditary spherocytosis in the same patient;Li;Exp Ther Med,2018
3. Homozygous ß-thalassemia (FCS8-AA) and hereditary spherocytosis in the same patient;Uysal;Turk J Haematol,2001
4. α-Thalassemia and hereditary spherocytosis in the same patient: the interaction of two diseases;Uysal;Pediatr Hematol Oncol,1998
5. Coexistence of hereditary spherocytosis (HS) due to band 3 deficiency and beta-thalassemia trait: partial correction of HS phenotype;Miraglia del Giudice;Br J Haematol,1993
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