Abstract
This article, the first of four in the series, is an introduction to the genetic inheritance, pathophysiology, and clinical manifestation of SCD and beta thalassaemia. The second and third papers focus on nursing assessment and clinical management of sickle cell disease and beta thalassaemia respectively, and the fourth outlines the revised genetic competencies for generalist midwives and for midwives and nurses who specialise in this area.
Original language | English |
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Journal | Nursing Times |
Volume | 00 |
Issue number | 00 |
Early online date | 16 Jun 2025 |
Publication status | E-pub ahead of print - 16 Jun 2025 |