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

Ralph HuitsAnne-Marie FeyensNiels LonnevilleXavier PeyrassolAnne-Sophie AdamBeatrice GulbisMarjan Van Esbroeck
Published in: Journal of clinical pathology (2022)
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.
Keyphrases
  • primary care
  • genome wide
  • sickle cell disease
  • risk factors
  • mitochondrial dna
  • copy number
  • smoking cessation
  • dna methylation
  • gene expression
  • human immunodeficiency virus
  • hiv infected
  • antiretroviral therapy