Diagnosis and clinical relevance of co-inheritance of haemoglobin D-Punjab/β+-thalassemia traits in an immigrant Afghan family-Reference-Cited by-同舟云学术

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

Published:2022-01-17 Issue:12 Volume:75 Page:861-864
ISSN:0021-9746
Container-title:Journal of Clinical Pathology
language:en
Short-container-title:J Clin Pathol

Author:

Huits Ralph^ORCID,Feyens Anne-Marie,Lonneville Niels,Peyrassol Xavier,Adam Anne-Sophie,Gulbis Beatrice,Van Esbroeck Marjan

Abstract

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.

Publisher

BMJ

Subject

General Medicine,Pathology and Forensic Medicine

Reference20 articles.

1. Hemoglobinopathies: clinical manifestations, diagnosis, and treatment;Kohne;Dtsch Ärzteblatt Int,2011

2. Gulbis B , Ferster A , Vertongen F , et al . Hemoglobinopathies in Belgium. Belg J Hematol 2010:50–6.

3. Inherited haemoglobin disorders: an increasing global health problem;Weatherall;Bull World Health Organ,2001

4. Strategies for basic laboratory diagnostics of the hemoglobinopathies in multi-ethnic societies: interpretation of results and pitfalls;Giordano;Int J Lab Hematol,2013

5. HbA2 measurements in β-thalassemia and in other conditions;Ivaldi;Thalassemia Reports,2014

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