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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...
保存先:
| 出版年: | J Int Med Res |
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| 主要な著者: | , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
SAGE Publications
2020
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7254599/ https://ncbi.nlm.nih.gov/pubmed/32212884 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/0300060520904849 |
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