A Child With Hereditary Spherocytosis Associated With Von Willebrand’s Disease: A Case Report From Saudi Arabia

Von Willebrand disease (VWD) is an autosomal inherited hemostasis disorder caused by a deficiency or defect in the blood protein known as von Willebrand factor, which is necessary for platelets to adhere to damaged vessel walls. The main symptoms of the condition include spontaneous bleeding from mu...

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Detalles Bibliográficos
Autores principales: Zolaly, Mohammed A, Alemam, Mariam M, Kheder, Omar M, Aljohani, Abdullah K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9617464/
https://www.ncbi.nlm.nih.gov/pubmed/36324358
http://dx.doi.org/10.7759/cureus.29733

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9617464/
https://www.ncbi.nlm.nih.gov/pubmed/36324358
http://dx.doi.org/10.7759/cureus.29733

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