Glanzmann Thrombasthenia report of a case and review of literature
Journal: University Journal of Surgery and Surgical Specialities (Vol.5, No. 10)Publication Date: 2019-12-02
Authors : VIGNESH C B;
Page : 7-9
Keywords : Glanzmann thrombasthenia; GPIIbIIIa receptor;
Abstract
Glanzmann thrombasthenia is an, autosomal recessive bleeding disorder associated with mutation of the gene for GPIIbIIIa receptor of the platelets, characterized by normal platelet count and morphology, with an abnormal platelet functional assay with increased bleeding time, normal coagulation profile,. It is a rare disorder with 1 in million incidence. Patients usually present with mucocutoneous bleeding and excessive bleeding associated with trauma or surgery, requiring blood and platelet transfusions. With proper supportive care Glanzmanns thrombasthenia has a very good prognosis. We present this rare case with review of the literature.
Other Latest Articles
- Role of CPP-ACP in preventing white spot lesions – A Short Review
- KNOWLEDGE, ATTITUDE AND PRACTICE OF GLAUCOMA AMONG THE HOSPITAL WORKERS IN A TEACHING HOSPITAL
- The Adrenergic Mechanism in the Implementation of the Cholinergic Anti-Inflammatory Pathway | Biomedgrid
- Coulomb’s Law Stand to The World of Elementary Particles in the Way That Newton’s Laws of Classical Mechanics Stand to The Macroscopic World | Biomedgrid
- What the Next Bioethics law says about us | Biomedgrid
Last modified: 2019-12-02 16:47:21