Rare Late Presentation of Severe Congenital Hemophilia A in a Ugandan Soldier - Case Report

dc.contributor.authorAtwiine, Barnabas
dc.contributor.authorAirewele, Gladstone
dc.date.accessioned2022-08-18T09:50:25Z
dc.date.available2022-08-18T09:50:25Z
dc.date.issued2022-03-30
dc.description.abstractPatients with severe hemophilia are usually diagnosed in infancy due to early onset of abnormal bleeding symptoms that characterize the disease. Affected individuals require coagulation factor routinely or prior to surgical procedures to prevent bleeding and are usually excluded from activities with a high risk of trauma. A 25-year old active-duty soldier was diagnosed with severe congenital hemophilia A after presenting with initial episode of prolonged bleeding. His case demonstrates a rare late presentation of a disease that typically presents in infancy and highlights the need for improving knowledge about bleeding disorders among health workers and the communityen_US
dc.identifier.citationAtwiine, B., & Airewele, G. (2022). Rare Late Presentation of Severe Congenital Hemophilia A in a Ugandan Soldier-Case Report. Authorea Preprints.en_US
dc.identifier.urihttp://ir.must.ac.ug/handle/123456789/2399
dc.language.isoen_USen_US
dc.publisherAuthorea Preprintsen_US
dc.subjectCongenital Hemophiliaen_US
dc.subjectCase Reporten_US
dc.subjectPatientsen_US
dc.subjectDiagnosisen_US
dc.titleRare Late Presentation of Severe Congenital Hemophilia A in a Ugandan Soldier - Case Reporten_US
dc.typeArticleen_US

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