DOAJ
Open Access
2025
Lessons from a qualitative study of treatment experiences and perceptions in people with haemophilia in France
Castet Sabine-Marie
Sepot-Boucherit Lola
Beranger Nicolas
Delienne Stephanie
Chamouard Valérie
Abstrak
Haemophilia A and B (HA/HB) are congenital, X-linked recessive bleeding disorders caused by deficiency of clotting factor VIII (FVIII) or IX (FIX), respectively. People with haemophilia (PwH) have increased risk of spontaneous or traumatic bleeding in joints, muscles, or soft tissues, which can be severe in people with HA/HB with inhibitors (HAwI/HBwI). Despite advances in haemophilia treatment, there are remaining and emerging unmet needs in PwH.
Topik & Kata Kunci
Penulis (5)
C
Castet Sabine-Marie
S
Sepot-Boucherit Lola
B
Beranger Nicolas
D
Delienne Stephanie
C
Chamouard Valérie
Akses Cepat
Informasi Jurnal
- Tahun Terbit
- 2025
- Sumber Database
- DOAJ
- DOI
- 10.2478/jhp-2025-0006
- Akses
- Open Access ✓