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: | , , , , , , |
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| Format: | Book |
| Published: |
LLC "MEDIAFORMAT",
2024-02-01T00:00:00Z.
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