Acute liver failure in a pediatric patient with congenital dyserythropoietic anemia type I treated with deferasirox
Congenital dyserythropoietic anemias (CDA) represent a heterogeneous group of disorders characterized by morphological abnormalities of erythroid precursor cells and various degrees of hemolysis. Iron overload is a result of continuous hemolysis and recurrent transfusions. It is treated with iron ch...
Main Authors: | Galina Ling, Vered Pinsk, Inbal Golan-Tripto, Eduard Ling |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2015-09-01
|
Series: | Hematology Reports |
Subjects: | |
Online Access: | http://www.pagepress.org/journals/index.php/hr/article/view/5987 |
Similar Items
-
Rare congenital Dyserythropoietic anemia of childhood: A case report
by: Hamzeh F. Al Hussien, et al.
Published: (2023-02-01) -
Congenital dyserythropoietic anemia type IV with kruppel-like factor 1 E325K mutation in a preterm neonate: Case and literature review
by: Reema Garegrat, et al.
Published: (2022-01-01) -
Congenital dyserythropoietic anemia in children: Case series with review of literature
by: Jasmita Dass, et al.
Published: (2024-06-01) -
Diagnosis: Congenital Dyserythropoietic Anemia Type 2 Due to Compound Heterozygote Mutation in SEC23B Gene
by: Fatih Demircioğlu, et al.
Published: (2015-07-01) -
Development of High-Resolution Melting Curve Analysis for rapid detection of SEC23B gene mutation causing Congenital Dyserythropoietic Anemia type II in Indian population
by: Arati Nandan Saptarshi, et al.
Published: (2023-07-01)