Α case of late diagnosis of compound heterozygosity for Hb Adana (HBA2:c.179G>A) in trans to an α+- thalassemia deletion: guilty or innocent

Background: Hemoglobin Adana is a non-deletional alpha chain mutation, particularly rare, and to date, it is mostly described in coinheritance to other a-thalassemia mutations. Such interactions result in various phenotypes depending on the underlying genotype. Since routine hematological tests do n...

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Detalles Bibliográficos
Publicado en:Hippokratia
Main Authors: Tampaki, A, Theodoridou, S, Apostolou, Ch, Delaki, EE, Vlachaki, E
Formato: Artigo
Idioma:Inglês
Publicado: SOCIETY OF "FRIENDS OF HIPPOKRATIA JOURNAL" 2020
Assuntos:
Case Report
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC7733358/
https://ncbi.nlm.nih.gov/pubmed/33364739
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