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...
Сохранить в:
| Главные авторы: | , , , , , , |
|---|---|
| Формат: | Статья |
| Язык: | английский |
| Опубликовано: |
Frontiers Media S.A.
2025-07-01
|
| Серии: | Frontiers in Pediatrics |
| Предметы: | |
| Online-ссылка: | https://www.frontiersin.org/articles/10.3389/fped.2025.1649183/full |
| Метки: |
Добавить метку
Нет меток, Требуется 1-ая метка записи!
|