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Clinical case of inhibitor form of hemophilia B in a child

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...

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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.
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Summary: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, clinically manifested by the presence of IgG allo-antibodies neutralizing exogenous FIX. The article describes a clinical case of an inhibitory form of hemophilia B in a 12-year-old child.
Item Description:10.47407/kr2023.5.2.00395
2713-2552

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