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Instructional Module for Nurses regarding Care of Children with Hemophilia
2018
Egyptian Journal of Health Care
Hemophilia is a coagulation disorder arising from a genetic defect of the X chromosome; the defect can either be inherited or result from spontaneous gene mutation. In each type of hemophilia (A, B, C, and willebrands disease), a critical coagulation protein is missing, causing children to bleed for long periods of time before clotting occurs. Aim: this study was a quasiexperimental aimed to evaluate the outcomes of the instructional module on the studied sample. Setting: the study was carried
doi:10.21608/ejhc.2018.16807
fatcat:3gfzsyi3ivhfbe7hgwuvi64lje