Coinheritance of Triplicated Alpha-Globin Gene and Beta-Thalassemia Mutations in Adulthood: Ten Years of Referrals in Northern Greece.

doi:10.1097/MPH.0000000000001730

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Article

Coinheritance of Triplicated Alpha-Globin Gene and Beta-Thalassemia Mutations in Adulthood: Ten Years of Referrals in Northern Greece.

Journal of pediatric hematology/oncology - 1 Nov 2020

Theodoridou Stamatia, Balassopoulou Angeliki, Boutou Effrossyni, Delaki Evangelia-Eleni, Yfanti Eleni, Vyzantiadis Timoleon-Achilleas, Vetsiou Evangelia, Voskaridou Ersi, Vlachaki Efthymia

Abstract excerpt

Greece is a country of ~11 million people, where hemoglobinopathies are the most common genetic diseases. The reported data describe the clinical phenotype of cases with coinheritance of triplicated α-globin (anti-α3.7 kb) and β-globin gene mutations in Northern Greece, that were referred within the last 10 years, in The Adult Thalassemia Unit of "Hippokration" Hospital, Thessaloniki, Northern Greece. The...

Topics

Adolescent
Adult
Aged
Aged, 80 and over
Female
Follow-Up Studies
Genotype
Greece
Humans
Male
Middle Aged

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Mutation

Phenotype

Prognosis

Referral and Consultation

Retrospective Studies

Young Adult

alpha-Globins

Source

Open in PubMed

Identifiers

PMID: 32032239
DOI: 10.1097/MPH.0000000000001730

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