A. Ariano

PO096 | IDENTIFICATION OF A NEW VARIANT IN THE RASGRP2 GENE IN A CHILD WITH SUSPECTED GLANZMANN THROMBASTHENIA

Introduction. Congenital platelet disorders constitute a heterogeneous group of primary hemostatic defects that are often difficult to diagnose without an integrated approach that includes functional testing. We report the case of a child with suspected Glanzmann thrombasthenia, in whom a novel variant of the RasGRP2 g...