Atypical acquired hemophilia linked with primary biliary cholangitis: a unique case presentation

Acquired hemophilia A is an uncommon disease often presented with bleeding episodes causing a significant mortality risk. The main responsible for the threatening hemorrhagic disorder is the Factor VIII autoantibody’s development. Acquired inhibitors’ presence is frequently idiopathic, but it can be...

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Autori principali:	Fatma Megdiche, Nour Siala, Faten Kallel, Imen Krichen, Hend Hachicha, Imen Frikha, Maha Charfi, Naourez Kallel, Moez Medhaffar, Hatem Masmoudi, Moez Elloumi, Choumous Kallel
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	Taylor & Francis Group 2025-12-01
Serie:	Future Science OA
Soggetti:	Acquired hemophilia A activated partial thromboplastin time autoimmune diseases FVIII inhibitor hemorrhage primary biliary cholangitis
Accesso online:	https://www.tandfonline.com/doi/10.1080/20565623.2025.2489329
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