A Rare Thalassemic Syndrome Caused by Interaction of Hb Adana [α59(E8)Gly→Asp] with an α+-Thalassemia Deletion: Clinical Aspects in Two Cases-Reference-Cited by-同舟云学术

A Rare Thalassemic Syndrome Caused by Interaction of Hb Adana [α59(E8)Gly→Asp] with an α+-Thalassemia Deletion: Clinical Aspects in Two Cases

Published:2008-01 Issue:4 Volume:32 Page:361-369
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Douna Varvara,Papassotiriou Ioannis,Garoufi Anastasia,Georgouli Eleni,Ladis Vassilis,Stamoulakatou Alexandra,Metaxotou-Mavrommati Anna,Kanavakis Emmanuel,Traeger-Synodinos Joanne

Publisher

Informa UK Limited

Subject

Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology

Link

http://www.tandfonline.com/doi/pdf/10.1080/03630260802173890

Reference28 articles.

1. Distinct Phenotypic Expression Associated with a New Hyperunstable Alpha Globin Variant (Hb Heraklion, α1cd37(C2)Pro>0): Comparison to Other α-Thalassemic Hemoglobinopathies

2. The Thalassemia Repository (Ninth Edition; Part II)

3. Unstable alpha-chain hemoglobin variants with factitious beta-thalassemia biosynthetic ratio: Hb questembert (α131[H14] Ser→Pro) and Hb Caen (α132[H15] Val→Gly)

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1. Hb F-Wentzville [Gγ24(B6)Gly→Glu; HBG2: c.74G>A, p.Gly25Glu]: An Unstable Gγ-Globin Variant Associated with Neonatal Hemolytic Anemia;Hemoglobin;2020-01-02

2. Thalassemia major phenotype caused by HB Zürich-Albisrieden [α2 59(E8) Gly > Arg (HBA2:C.178G > C)] in a Brazilian child;Pediatric Blood & Cancer;2018-08-27

3. Hb Adana (HBA2 or HBA1: c.179G > A) and alpha thalassemia: Genotype-phenotype correlation;Pediatric Blood & Cancer;2018-05-11

4. Molecular basis of α-thalassemia;Blood Cells, Molecules, and Diseases;2018-05

5. Compound Heterozygosity for Hb Adana (HBA2: c.179G>A) and the –α3.7/αα Thalassemia Deletion in Greece: Clinical Phenotype and Genetic Counseling;Hemoglobin;2018-03-04