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    State-of-the-Art Session

    Hemophilia and Rare Bleeding Disorders

    What Do We Do When the Cause of the Bleeding Is Unclear?

    SOA 14.1 - What Goes Unseen: Unrecognized Inheritance Contributing to Bleeding in Rare Bleeding Disorders and Hemophilia

    Monday, June 26, 2023
    08:00 – 08:25 ET
    Room: 710A
    Session Available As: On-Demand
    Please view the 2023 RPTH State-of-the-Art Illustrated Capsules here.

    Learning Objectives:

    • understand the importance of screening for additional molecular variants when sequencing rare clotting protein genes
    • recognize how certain pathologic genetic variants may nnot be identified accurately with current clinical laboratory assays.
    • identify the important role of modifying gene variants in determining clotting protein expression and platelet function