Glanzmann's Thrombasthenia: A rare platelet functional disorder
DOI:
https://doi.org/10.3329/fmcj.v15i2.53898Keywords:
Glanzmann's Thrombasthenia (GT)Abstract
Glanzmann's Thrombasthenia (GT) is a rare inherited autosomal recessive platelet functional disorder. Due to the deficiency of platelet function, it manifests as a bleeding disorder characterized by mucocutaneous hemorrhage of varying severity. It is difficult to diagnose as it closely mimics with others bleeding disorder, so it can be diagnosed after investigations & exclusion of others. Treatment is supportive care with platelet transfusion & proper counseling. With careful supportive care, GT has a very good prognosis. In this report, we describe a 13 years old female with Glanzmann Thrombasthenia.
Faridpur Med. Coll. J. 2020;15(2): 103-105
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Published
2021-06-08
How to Cite
Kamruzzaman, M., Hossain, M. I., Rahman, M. A., & Sharifunnesa, .-. (2021). Glanzmann’s Thrombasthenia: A rare platelet functional disorder. Faridpur Medical College Journal, 15(2), 103–105. https://doi.org/10.3329/fmcj.v15i2.53898
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Case Reports