Multidisciplinary approaches to coexisting Glanzmann thrombasthenia and juvenile polyposis syndrome
Glanzmann thrombasthenia (GT) is a rare autosomal recessive bleeding disorder from defects in the αIIbβ3 integrin receptor, impairing platelet aggregation and often overlooked due to normal platelet counts. Juvenile polyposis syndrome (JPS) is an autosomal dominant disorder with multiple gastrointes...
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| Hlavní autoři: | , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Elsevier
2026-01-01
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| Edice: | Leukemia Research Reports |
| Témata: | |
| On-line přístup: | http://www.sciencedirect.com/science/article/pii/S2213048926000233 |
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