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  2. Haemophilia - Wikipedia

    en.wikipedia.org/wiki/Haemophilia

    Children with mild to moderate haemophilia may not have any signs or symptoms at birth, especially if they do not undergo circumcision. Their first symptoms are often frequent and large bruises and haematomas from frequent bumps and falls as they learn to walk. Swelling and bruising from bleeding in the joints, soft tissue, and muscles may also ...

  3. Haemophilia B - Wikipedia

    en.wikipedia.org/wiki/Haemophilia_B

    Haemophilia B, also spelled hemophilia B, is a blood clotting disorder causing easy bruising and bleeding due to an inherited mutation of the gene for factor IX, and resulting in a deficiency of factor IX. It is less common than factor VIII deficiency (haemophilia A). [3]

  4. Here’s Why You Bruise So Easily, According to a Doctor - AOL

    www.aol.com/why-bruise-easily-according-doctor...

    Long-term steroid use, on the other hand, causes thinning of the skin, making it more susceptible to bruising. That same logic applies to older folks’ tendency to bruise like a peach.

  5. Haemophilia C - Wikipedia

    en.wikipedia.org/wiki/Haemophilia_C

    Hemophilia C; Other names: Plasma thromboplastin antecedent (PTA) deficiency, Rosenthal syndrome: Haemophilia C caused by deficiency in Factor XI [1] Specialty: Haematology: Symptoms: Oral bleeding [2] Causes: Deficiency of coagulation factor XI [1] Diagnostic method: Prothrombin time [1] Prevention: Physical activity precautions [1] Treatment ...

  6. Haemophilia A - Wikipedia

    en.wikipedia.org/wiki/Haemophilia_A

    Hemophilia A: Protein structure of coagulation factor VIII, of which its deficiency is the cause of haemophilia A. Specialty: Haematology: Symptoms: Prolonged bleeding from common injuries [1] Causes: Factor VIII deficiency [2] Diagnostic method: Bleeding time, [2] coagulation screen, genetic testing: Prevention: Hepatitis B vaccine should be ...

  7. List of hematologic conditions - Wikipedia

    en.wikipedia.org/wiki/List_of_hematologic_conditions

    The cause for the disorder is related to a genetic mutation of the HBB gene. This gene is responsible for providing the instructions to produce beta-globin; one of the major components of hemoglobin. The two classification types of beta thalassemia are thalassemia major (also known as Cooley's anemia) and thalassemia intermedia.