Von Willebrand's disease: case report and review of literature

Von Willebrand Disease (VWD) is the most common human inherited bleeding disorder due to a defect of Von Willebrand Factor (VWF), which a glycoprotein crucial for platelet adhesion to the subendothelium after vascular injury. VWD include quantitative defects of VWF, either partial (type 1 with VWF l...

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Dettagli Bibliografici
Pubblicato in:Pan Afr Med J
Autori principali: Echahdi, Hanae, El Hasbaoui, Brahim, El Khorassani, Mohamed, Agadr, Aomar, Khattab, Mohamed
Natura: Artigo
Lingua:Inglês
Pubblicazione: The African Field Epidemiology Network 2017
Soggetti:
Case Report
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5567960/
https://ncbi.nlm.nih.gov/pubmed/28904675
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.11604/pamj.2017.27.147.12248
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