Clinical case of inhibitor form of hemophilia B in a child

• Main Authors: Alexandra V. Serezhkina (Author), Irina G. Khmelevskaya (Author), Natalya S. Razinkova (Author), Irina I. Zhiznevskaya (Author), Tatyana A. Minenkova (Author), Tatyana V. Feoktistova (Author), Maxim P. Ivenkov (Author)
• Format: Book
• Published: LLC "MEDIAFORMAT", 2024-02-01T00:00:00Z.
• Subjects: article
• Online Access: 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...