Case report of recurrent bleeding in an infant with isolated prolonged prothrombin time due to congenital factor VII deficiency---a riddle solved

Factor VII deficiency is a rare bleeding disorder showing an autosomal recessive pattern of inheritance. Data from our country on this particular entity is lacking. Especially the specific mutations associated with this disease are not well documented. The disease can have a wide spectrum of present...

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Detalles Bibliográficos
Autores principales: Ganguly, Mimi, Sutradhar, Saurabh, Rajbangshi, Arghya, Pattnaik, Amrita, Maiti, Dipshikha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9480649/
https://www.ncbi.nlm.nih.gov/pubmed/36119192
http://dx.doi.org/10.4103/jfmpc.jfmpc_965_21

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9480649/
https://www.ncbi.nlm.nih.gov/pubmed/36119192
http://dx.doi.org/10.4103/jfmpc.jfmpc_965_21

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