Abstract
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.
Key words: hemophilia B, inhibitory form, children, hematology
For citation:Serezhkina A.V., Khmelevskaya I.G., Razinkova N.S., Zhiznevskaya I.I., Minenkova T.A., Feoktistova T.V., Ivenkov M.P. Clinical case of inhibitor form of hemophilia B in a child. Clinical analysis in general medicine. 2024; 5 (2): 98–100 (In Russ.). 98–100. DOI: 10.47407/ kr2023.5.2.00395
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