Comprehensive Center forBleeding Disorders
Hemophilia is an inherited bleeding disorder caused by a deficiency or dysfunction of blood-clotting factors. Hemophilia A results from factor VIII deficiency, while hemophilia B stems from factor IX deficiency. We provide comprehensive hemophilia management, from prophylactic factor replacement to breakthrough therapies like gene therapy for hemophilia B. Our team helps patients navigate treatment options, optimize dosing regimens, manage bleeding episodes, and maintain joint health through both traditional factor replacement and extended half-life products.
Von Willebrand disease is the most common inherited bleeding disorder, caused by a deficiency or dysfunction of von Willebrand factor, a protein essential for normal blood clotting. Accurate diagnosis requires sophisticated laboratory testing and clinical expertise, both of which our team provides. We distinguish between disease types and subtypes, enabling precise treatment selection including desmopressin therapy, von Willebrand factor replacement products, and strategies for managing bleeding during surgery, dental procedures, and childbirth.
Platelet function disorders affect the ability of platelets to properly adhere, activate, and aggregate at sites of blood vessel injury. We provide specialized platelet function testing to accurately diagnose these often-subtle conditions. Our treatment approaches are highly individualized, taking into account each patient's specific platelet defect, bleeding history, and lifestyle factors.
Thrombophilia refers to conditions that increase the risk of developing abnormal blood clots in veins or arteries. These conditions can be inherited, such as factor V Leiden or a prothrombin gene mutation, or acquired, like antiphospholipid syndrome. We provide comprehensive evaluation to identify underlying clotting disorders, helping patients and their physicians understand clot risk and make informed decisions about anticoagulation therapy while balancing clot prevention with bleeding risk.
We diagnose and manage rare bleeding disorders, including deficiencies of factors I, II, V, VII, X, XI, and XIII, as well as combined factor deficiencies and rare platelet disorders like Bernard-Soulier syndrome and Glanzmann thrombasthenia. Our team has expertise in these uncommon conditions, providing accurate diagnosis, personalized treatment planning and connections to national and international rare disease networks.