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article · PLoS ONE

Clinical and laboratory characterization of adult sickle cell anemia patients in Kinshasa

20228 citationsOpen accessUniversité de Kinshasa (UNIKIN)

Abstract

In this selected, hospital-based populations of adults with SCA, severe disease was rare, which may be due to survival bias. However, two thirds had moderate severity of the disease, mostly with a low HbF, and they may benefit from HU treatment. In the Central-African setting the separation between vaso-occlusive and hyperhemolytic sub-phenotypes was not applicable.

Research topics

  • Hemoglobinopathies and Related Disorders
  • Iron Metabolism and Disorders
  • Prenatal Screening and Diagnostics

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DOI: 10.1371/journal.pone.0278478

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