Clinical case of inhibitor form of hemophilia B in a child

• Hauptverfasser: Alexandra V. Serezhkina (Verfasst von), Irina G. Khmelevskaya (Verfasst von), Natalya S. Razinkova (Verfasst von), Irina I. Zhiznevskaya (Verfasst von), Tatyana A. Minenkova (Verfasst von), Tatyana V. Feoktistova (Verfasst von), Maxim P. Ivenkov (Verfasst von)
• Format: Buch
• Veröffentlicht: LLC "MEDIAFORMAT", 2024-02-01T00:00:00Z.
• Schlagworte: article
• Online-Zugang: Connect to this object online.

Hemophilia B is a hereditary, X-linked recessive disease caused by a violation of plasma homeostasis, resulting from a deficiency or absence of coagulation factor IX (FIX). The cause is a mutation of the Xq27 gene encoding FIX. A serious complication of this pathology is the inhibitory form, clinica...