Development of an FVIII Inhibitor in a Mild Hemophilia Patient with a Phe595Cys Mutation

Mild hemophilia A is caused by a missense mutation in the FVIII gene that is responsible for a decrease in the FVIII:C to between 5% and 40%. The development of FVIII inhibitors has been reported in 3-13% of patients with mild hemophilia. Genetic risk factors for the development of inhibitors in mil...

Descripción completa

Detalles Bibliográficos
Autores principales: Yamanouchi, Jun, Tokumoto, Daiki, Ikeda, Yuichi, Maruta, Masaki, Kaneko, Masahiko, Hato, Takaaki, Yasukawa, Masaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Internal Medicine 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6262709/
https://www.ncbi.nlm.nih.gov/pubmed/29877292
http://dx.doi.org/10.2169/internalmedicine.1145-18

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6262709/
https://www.ncbi.nlm.nih.gov/pubmed/29877292
http://dx.doi.org/10.2169/internalmedicine.1145-18

Ejemplares similares