Diagnosis and clinical relevance of co-inheritance of haemoglobin D-Punjab/β+-thalassemia traits in an immigrant Afghan family

We report on a Pashtun family affected by haemoglobin D-Punjab/β+-thalassemia to increase the awareness of the increasing prevalence of haemoglobinopathies among primary care physicians. We highlight the diagnostic approach of these conditions and the benefits of genetic counselling.

Detalles Bibliográficos
Autores principales: Huits, Ralph, Feyens, Anne-Marie, Lonneville, Niels, Peyrassol, Xavier, Adam, Anne-Sophie, Gulbis, Beatrice, Van Esbroeck, Marjan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2022
Materias:
Short Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9685697/
https://www.ncbi.nlm.nih.gov/pubmed/35039448
http://dx.doi.org/10.1136/jclinpath-2021-208009

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9685697/
https://www.ncbi.nlm.nih.gov/pubmed/35039448
http://dx.doi.org/10.1136/jclinpath-2021-208009

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