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This article discusses the inherited bleeding disorder hemophilia that results from improper functioning of the clotting factors VIII (hemophilia A) or IX (hemophilia B). The disorder could manifest in children with repeated bleeding episodes, hemarthrosis, muscle hematoma, and severe bleeding episodes. With timely diagnosis and adequate therapy, it is possible to prevent complications, maintain the joint function, and enhance the quality of life. The purpose of this review is to analyze the studies regarding the clinical manifestations of hemophilia, approaches, complications, and treatment methods.
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Begimai Muktarali kyzy (2026) studied this question.
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