Concurrent Deficiency of Factor V and Factor VIII in a Pediatric Patient: A Case Report

This case report delves into an uncommon coagulopathy recognized as factor V and VIII deficiency (F5F8D), which follows an autosomal recessive inheritance pattern. The focal point of this study is a five-year-old Asian female who was initially presented with complaints of hematuria, epistaxis, and b...

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Detalles Bibliográficos
Autores principales: Rahman, Tanzeel U, Salih, Noman, Rashid, Nasar, Ahmad, Maaz, Khan, Asad, Yousufi, Zainab
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10589818/
https://www.ncbi.nlm.nih.gov/pubmed/37868465
http://dx.doi.org/10.7759/cureus.45663

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10589818/
https://www.ncbi.nlm.nih.gov/pubmed/37868465
http://dx.doi.org/10.7759/cureus.45663

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