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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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Ngā kaituhi matua:	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)
Hōputu:	Pukapuka
I whakaputaina:	LLC "MEDIAFORMAT", 2024-02-01T00:00:00Z.
Ngā marau:	article
Urunga tuihono:	Connect to this object online.
Ngā Tūtohu:	Tāpirihia he Tūtohu Kāore He Tūtohu, Me noho koe te mea tuatahi ki te tūtohu i tēnei pūkete!

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