Please use this identifier to cite or link to this item:
http://20.193.157.4:9595/xmlui/handle/123456789/1606Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Raghavendra H Gobbur, Issac Varghese | - |
| dc.date.accessioned | 2020-01-07T10:12:05Z | - |
| dc.date.available | 2020-01-07T10:12:05Z | - |
| dc.date.issued | 2014 | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/1606 | - |
| dc.description.abstract | 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). | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | BLDE(Deemed to be University) | en_US |
| dc.subject | Epistaxis; Glanzmann's Thrombasthenia; Recurrent Epistaxis | en_US |
| dc.title | Rare case of glanzmann thrombastenia. | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | Faculty of Pediatrics | |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.