{"id":11479,"date":"2025-07-26T16:56:57","date_gmt":"2025-07-26T14:56:57","guid":{"rendered":"https:\/\/valintermed.com\/?p=11479"},"modified":"2025-07-26T16:56:57","modified_gmt":"2025-07-26T14:56:57","slug":"gemofiliya-a","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/gemophilia-a\/","title":{"rendered":"Hemophilia A"},"content":{"rendered":"
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Hemophilia A is an inherited blood disorder characterized by a deficiency of factor VIII, which leads to impaired hemostasis and an increased risk of hemorrhage. This inherited disorder is passed down through families and is often associated with mutations that affect specific genes. Hemophilia A occurs in varying degrees of severity, from a mild form in which a person can lead a virtually normal life to a severe form in which even minor injuries can lead to serious bleeding. Evaluation and treatment of this disorder require a multidisciplinary approach and the involvement of various health care professionals.<\/p>\n

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