Home|Journals|Articles by Year|Audio Abstracts
 

Case Report



A rare case of Glanzmann Thrombasthenia

Raghavendra HanumanthRao Gobbur, Issac Varghese.




Abstract
Cited by 5 Articles

Recurrent Epistaxis often is due to thrombocytopenia. Child with recurrent Epistaxis had abnormal bleeding time, coupled with normal platelet count congenital Glanzmann Thrombasthenia (GT) though rare is a possible condition. Severe bleeding in GT required platelet transfusions, and whole blood (as replacement for gross blood loss). Suspect Glanzmann Thrombasthenia, when recurrent Epistaxis with prolonged bleeding time is associated with normal platelet count. Mild bleeding is best treated with local and IV Tranexamic acid (30 mg / kg).

Key words: Epistaxis; Glanzmann's Thrombasthenia; Recurrent Epistaxis






Full-text options


Share this Article


Online Article Submission
• ejmanager.com




ejPort - eJManager.com
Refer & Earn
JournalList
About BiblioMed
License Information
Terms & Conditions
Privacy Policy
Contact Us

The articles in Bibliomed are open access articles licensed under Creative Commons Attribution 4.0 International License (CC BY), which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.