Glanzmann’s thrombasthenia with spontaneous upper gastrointestinal bleeding: a case report

Glanzmann’s thrombasthenia (GT) is a rare bleeding disorder inherited in an autosomal recessive manner. The pathogenesis of GT mainly involves structural abnormalities and dysfunction of platelet membrane glycoprotein IIb/IIIa (integrin αIIbβ3). The most common symptoms of GT are various types of bl...

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Detalles Bibliográficos
Autores principales: Qiao, Zhenguo, Chen, Yi, Shi, Wangtianyi, Yang, Jun, Song, Yi, Shen, Jiaqing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7254599/
https://www.ncbi.nlm.nih.gov/pubmed/32212884
http://dx.doi.org/10.1177/0300060520904849

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7254599/
https://www.ncbi.nlm.nih.gov/pubmed/32212884
http://dx.doi.org/10.1177/0300060520904849

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