Thankam, Thamari and John, Ashnah (2024) Glanzmann’s Thrombasthenia: Report of A Case and Review of the Literature. International Journal of Life Sciences, 13 (2). pp. 38-40. ISSN 2277-193x
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Abstract
Glanzmann’s thrombasthenia (GT)is a rare autosomal recessive disorder characterized by qualitative or quantitative abnormalities of the platelet membrane glycoprotein (GP) IIb/IIIa. These integrins are encoded by the ITGA2B and ITGB3 genes and form platelet glycoprotein (GP)IIb/IIIa, which acts as the principal platelet receptor for fibrinogen. Spontaneous mucocutaneous bleeding is common and can lead to fatal bleeding episodes.
| Item Type: | Article |
|---|---|
| Uncontrolled Keywords: | Glanzmann’s thrombasthenia ,Glycoprotein, platelet, bleeding. |
| Subjects: | R Medicine > RT Nursing |
| Divisions: | Department of Community Health Nursing > Research papers |
| Depositing User: | ePrints Editor |
| Date Deposited: | 21 Aug 2025 17:38 |
| Last Modified: | 21 Aug 2025 17:38 |
| URI: | https://eprints.cihanuniversity.edu.iq/id/eprint/4452 |
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