Pathogenesis and treatment of osteoporosis in patients with hemophilia

INTRODUCTION: Hemophilia is a rare X-linked recessive inherited bleeding disorder caused by mutations of the genes encoding coagulation factor VIII (FVIII) or IX (FIX). Patients with hemophilia (PWH) often have a high risk of osteoporosis and fractures that is usually ignored. Herein, we review the...

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Detalles Bibliográficos
Autores principales: Lin, Xiaoyun, Gao, Peng, Zhang, Qian, Jiang, Yan, Wang, Ou, Xia, Weibo, Li, Mei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer London 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9813251/
https://www.ncbi.nlm.nih.gov/pubmed/36598583
http://dx.doi.org/10.1007/s11657-022-01203-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9813251/
https://www.ncbi.nlm.nih.gov/pubmed/36598583
http://dx.doi.org/10.1007/s11657-022-01203-9

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