Glanzmann Thrombasthenia – A Rare Case Report

Authors

  • Sabrina Rahman Junior Consultant, Department of Transfusion Medicine, BIHS General Hospital, Dhaka, Bangladesh
  • Maha Harun Junior Consultant, Department of Transfusion Medicine, Impulse Hospital, Dhaka, Bangladesh
  • Tashmim Farhana Dipta Professor and Head, Department of Transfusion Medicine & Clinical Haematology, BIRDEM General Hospital, Dhaka, Bangladesh
  • Farida Parvin Assistant Professor, Department of Transfusion Medicine & Clinical Haematology, BIRDEM General Hospital, Dhaka, Bangladesh

DOI:

https://doi.org/10.3329/dmcj.v9i2.74874

Keywords:

Thrombasthenia, Ecchymosis, Platelet, BIRDEM

Abstract

Glanzmann thrombasthenia is a rare inherited bleeding disorder resulting from mutation in platelet membrane glycoprotein (GP) IIb or IIIa leading to impaired platelet function which is characterized by defective platelet aggregation and diminished clot retraction. Glanzmann thrombasthenia patients commonly visit to physician with features of bleeding. Here we discuss about the case of a 32-years-old young female presented with menorrhagia, ecchymosis and occasional gum bleeding. Her coagulation profile was in favor of Glanzmann thrombasthenia. This rare disease has a good outcome if early diagnosis and proper management can be ensured.   

Delta Med Col J. Jan 2021;9(2): 101-103 

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Published

2024-07-14

How to Cite

Rahman, S., Harun, M., Dipta, T. F., & Parvin, F. (2024). Glanzmann Thrombasthenia – A Rare Case Report. Delta Medical College Journal, 9(2), 101–103. https://doi.org/10.3329/dmcj.v9i2.74874

Issue

Vol. 9 No. 2 (2021)

Section

Case Reports

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Articles in the Delta Medical College Journal are Open Access articles published under a Creative Commons Attribution 4.0 International License CC BY License.

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