Over time, individuals with hemophilia may experience recurrent bleeding episodes, which can lead to joint damage, chronic pain, and reduced mobility due to hemarthrosis (bleeding into joints). They are also at increased risk for life-threatening bleeding after injuries or surgeries. If not effectively managed with factor replacement therapies, hemophilia can significantly impact overall health and quality of life. Regular medical care and monitoring are essential to mitigate these risks.
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Hemophilia is a genetic disorder that has been present throughout history. However, it gained more recognition and understanding in the 19th century when it was first systematically described and studied by physicians. The ability to diagnose and manage hemophilia has improved over time with advances in medical knowledge and treatment options.
The are sujects to hemophilia, hemoraggies and other diseases.
It is estimated that about 20,000 males in the US are currently living with hemophilia. Hemophilia is a rare genetic blood disorder that primarily affects males. Treatment and management of hemophilia have significantly improved over the years.
Hemophilia A is an X-linked, hereditary bleeding disorder caused by the absence or defect of a blood clotting protein, Factor VIII. As a result, when a person with hemophilia A has a bleeding episode, the bleeding may be prolonged due to the body's inability to form blood clots. Patients who are affected with hemophilia A experience frequent spontaneous bleeding, most commonly into their joints and soft tissues, with bleeding into vital organs that may ... be life-threatening. Bleeding episodes may be painful, and over time, recurrent joint bleeding may result in debilitating destruction of the joints. Currently, patients with hemophilia A are dependent on injections of Factor VIII produced by genetic engineering or purified from human plasma, to help control a bleeding episode. It is estimated that approximately 50,000 individuals worldwide are affected with hemophilia A. Hemophilia A - Clotting Factor VIII Hemophilia B - Clotting Factor IX Hemophilia C - Clotting Factor XI
Hemophilia.
Hemophilia is one disease in which blood does not clot normally. von Willebrand's Disease
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There is no chance that the child will have hemophilia even if the spouse has hemophilia. Any girls the couple has will be carriers if the spouse has hemophilia.
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