{"id":11480,"date":"2025-07-26T16:56:25","date_gmt":"2025-07-26T14:56:25","guid":{"rendered":"https:\/\/valintermed.com\/?p=11480"},"modified":"2025-07-26T16:56:25","modified_gmt":"2025-07-26T14:56:25","slug":"gemofiliya-v","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/gemophilia-v\/","title":{"rendered":"Hemophilia B"},"content":{"rendered":"
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Hemophilia B is an inherited disorder caused by a deficiency of the clotting factor IX. As a result of this deficiency, patients have an increased susceptibility to bleeding, even with minor trauma. Hemophilia B, also known as Von dermatitis, is traditionally inherited through the X chromosome, making males more susceptible to the disorder, while females are more likely to be carriers. The disorder occurs in a variety of forms, including mild, moderate, and severe cases, with varying degrees of bleeding disorders. A precise understanding of the pathophysiology, genetic aspects of treatment options, and early diagnosis are key to successfully managing the health of patients with hemophilia B.<\/p>\n

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