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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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Bibliografische Detailangaben
Hauptverfasser: Sondus Alsharidah, Eman Almatter, Hana' Nofal, Maha Bourusly, Mohammad Obaid
Format: Artigo
Sprache:Inglês
Veröffentlicht: Elsevier 2026-01-01
Schriftenreihe:Leukemia Research Reports
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Online-Zugang:http://www.sciencedirect.com/science/article/pii/S2213048926000233
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