A RARE CASE OF GLANZMANN THOMBASTHENIA

Background: Glanzmanns Thrombasthenia (GT) is a GPIIb/IIIa platelet surface receptor condition that defined by lack of aggregation, either qualitatively or quantitatively. This receptors physiological function to bind various sticky plasma proteins aid adhesion and ensuring the development thrombus at sites vascular damage. Patient GT typically presents with menorrhagia, easy bruising, epistaxis, gum bleeding.Prolonged untreated unsuccessfully treated hemorrhagia associated GlanzmannsThrombasthenia may be life threatening. Case Description: A 12 years old girl presented bleeding since days complaints generalized weakness. The patient was then investigated find cause puberty menorrhagia. Several blood investigations were performed, final diagnosis made. Objective:To highlight rare case β-Thalassemia trait in