Back وهن صفيحات لغلانزمان Arabic Tromboastènia Catalan Glanzmann-Thrombasthenie German Trombastenia de Glanzman Spanish Thrombasthénie de Glanzmann French תרומבאסתניה על-שם גלנצמן HE Tromboastenia di Glanzmann Italian 血小板無力症 Japanese Ziekte van Glanzmann Dutch Trombastenia Glanzmanna Polish
| Glanzmann's thrombasthenia | |
|---|---|
| Other names | Thrombasthenia of Glanzmann and Naegeli[1] |
 | |
| This condition is inherited in a autosomal recessive manner | |
| Specialty | Hematology  |
Glanzmann's thrombasthenia is an abnormality of the platelets.[2] It is an extremely rare coagulopathy (bleeding disorder due to a blood abnormality), in which the platelets contain defective or low levels of glycoprotein IIb/IIIa (GpIIb/IIIa), which is a receptor for fibrinogen. As a result, no fibrinogen bridging of platelets to other platelets can occur, and the bleeding time is significantly prolonged.
- ^ "Glanzmann thrombasthenia | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". rarediseases.info.nih.gov. Archived from the original on 30 October 2019. Retrieved 30 October 2019.
- ^ "Glanzmann thrombasthenia" at Dorland's Medical Dictionary
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