https://doi.org/10.4081/btvb.2024.134

ReDIP, the Italian network for the diagnosis of congenital platelet function disorders

Vol. 3 No. 1 (2024)
Published: 22 April 2024
ReDIP, congenital platelet function disorders
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Authors

Marco Cattaneo
marco.natale.cattaneo@gmail.com
https://orcid.org/0000-0002-7343-4534
Fondazione Arianna Anticoagulazione, Bologna; Dipartimento di Scienze della Salute, Università degli Studi di Milano, Italy.
Claudia Ghali
https://orcid.org/0000-0003-3124-3403
Dipartimento di Scienze della Salute, Università degli Studi di Milano, Italy.
Mariangela Scavone
https://orcid.org/0000-0002-8421-0210
Dipartimento di Scienze della Salute, Università degli Studi di Milano, Italy.

Congenital platelet function disorders (cPFD) are associated with an increased risk of mucocutaneous bleeding of various levels of severity; they may be classified based on abnormalities of platelet components that share common characteristics: i) platelet receptors for adhesive proteins; ii) platelet receptors for soluble agonists; iii) platelet granules; iv) signal transduction pathways; v) procoagulant phospholipids; less well characterized PFD aregrouped in a sixth category of miscellaneous abnormalities [...].

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How to Cite

Cattaneo, M., Ghali, C., & Scavone, M. (2024). ReDIP, the Italian network for the diagnosis of congenital platelet function disorders. Bleeding, Thrombosis and Vascular Biology, 3(1). https://doi.org/10.4081/btvb.2024.134
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