Progressive cephalohematoma in a neonate revealing severe hemophilia a owing to intron 22 inversion: a case report

Progressive cephalohematoma in a neonate revealing severe hemophilia a owing to intron 22 inversion: a case report

BackgroundHemophilia A is a rare X-linked recessive bleeding disorder characterized by coagulation factor VIII (FVIII) deficiency or dysfunction. While most cases present during early childhood with joint or soft tissue bleeding, neonatal-onset hemophilia A is uncommon and often difficult to diagnos...

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Bibliographic Details
Main Authors: Cheng Peng, Qiuyue Kou, Qianqian Xia, Zhongfen Cao, Lili Liu, Xinlin Hou, Zezhong Tang
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-07-01
Series:Frontiers in Pediatrics
Subjects:
hemophilia A
cephalohematoma
neonate
F8 gene
emicizumab
Online Access:https://www.frontiersin.org/articles/10.3389/fped.2025.1649183/full
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