Concomitant Presence of Hb Agrinio and - -Med Deletion in a Greek Male Patient with Hemoglobinopathy H: More Severe Phenotype and Literature Review

Concomitant Presence of Hb Agrinio and - -Med Deletion in a Greek Male Patient with Hemoglobinopathy H: More Severe Phenotype and Literature Review

Hemoglobin (Hb) Agrinio is a rare non-deletional a-globin mutation observed almost exclusively in Greek, Spanish or other Mediterranean families. The clinical manifestations of a carrier of a single Hb Agrinio mutation (single heterozygosity) depend on the concomitant presence or absence of other mu...

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Bibliographic Details
Main Authors: Michael D. Diamantidis, Stefania Pitsava, Omar Zayed, Ioanna Argyrakouli, Konstantinos Karapiperis, Christos Chatzoulis, Evangelos Alexiou, Achilles Manafas, Evangelos Tsangalas, Konstantinos Karakoussis
Format: Article
Language:English
Published: MDPI AG 2023-08-01
Series:Hematology Reports
Subjects:
hemoglobinopathy H (HbH)
hemoglobin (Hb) agrinio
alpha thalassemia
severe clinical manifestations
chronic hemolysis
Online Access:https://www.mdpi.com/2038-8330/15/3/50

Internet

https://www.mdpi.com/2038-8330/15/3/50

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