Letters to the Editor
Vol. 3 No. 1 (2024)
ReDIP, the Italian network for the diagnosis of congenital platelet function disorders
Publisher's note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.
Published: 22 April 2024
468
Views
149
Downloads
Authors
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 [...].
Downloads
Download data is not yet available.
Citations
Cattaneo M. Inherited platelet-based bleeding disorders. J Thromb Haemost 2003;:1628-36 DOI: https://doi.org/10.1046/j.1538-7836.2003.00266.x
Quiroga T, Goycoolea M, Panes O, et al. High prevalence of bleeders of unknown cause among patients with inherited mucocutaneous bleeding. A prospective study of 280 patients and 299 controls. Haematologica 2007;92:357-65 DOI: https://doi.org/10.3324/haematol.10816
Rodeghiero F, Castaman G, Dini E. Epidemiological investigation of the prevalence of von Willebrand's disease. Blood 1987;69:454-9 DOI: https://doi.org/10.1182/blood.V69.2.454.454
Rodeghiero F, Tosetto A, Abshire T, et al. ISTH/SSC bleeding assessment tool: a standardized questionnaire and a proposal for a new bleeding score for inherited bleeding disorders. J Thromb Haemost 2010;8:2063-5 DOI: https://doi.org/10.1111/j.1538-7836.2010.03975.x
Lowe GC, Lordkipanidzé M, Watson SP et al. Utility of the ISTH bleeding assessment tool in predicting platelet defects in participants with suspected inherited platelet function disorders. J Thromb Haemost 2013;11:1663-8 DOI: https://doi.org/10.1111/jth.12332
Podda GM, Bucciarelli P, Lussana F et al. Usefulness of PFA-100 testing in the diagnostic screening of patients with suspected abnormalities of hemostasis: comparison with the bleeding time. J Thromb Haemost. 2007;5:2393-8 DOI: https://doi.org/10.1111/j.1538-7836.2007.02752.x
Cattaneo M. Congenital disorders of platelet function. In: AD Michelson, ed. Platelets, 3rd editon. San Diego, CA: Elsevier/Academic Press; 2013. pp 1019-47 DOI: https://doi.org/10.1016/B978-0-12-387837-3.00050-X
How to Cite
1.
Cattaneo M, Ghali C, Scavone M. ReDIP, the Italian network for the diagnosis of congenital platelet function disorders. Bleeding Thromb Vascul Biol [Internet]. 2024 Apr. 22 [cited 2025 Nov. 9];3(1). Available from: https://www.btvb.org/btvb/article/view/134
Copyright (c) 2024 The Author(s)
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
Share
Similar Articles
- CO11 | Oral anticoagulation with vitamin K antagonists in early childhood: a single centre-experience , Bleeding, Thrombosis and Vascular Biology: Vol. 4 No. s1 (2025)
- CO49 | The burden of cerebral small vessel disease in ITTP patients from acute phase to remission , Bleeding, Thrombosis and Vascular Biology: Vol. 4 No. s1 (2025)
- CO10 | Multidimensional risk assessment of venous thromboembolism (risk): an observational study comparing the Padua prediction score, Barthel index, and quality of life in hospitalized patients , Bleeding, Thrombosis and Vascular Biology: Vol. 4 No. s1 (2025)
- CS06 | Patient specific iPSCs-derived sinusoidal endothelial cells for phenotypic correction of haemophilia A , Bleeding, Thrombosis and Vascular Biology: Vol. 4 No. s1 (2025)
- CO52 | The impact of KRAS mutations on the risk of recurrent venous thromboembolism in patients with cancer-associated thrombosis and gastrointestinal neoplasms , Bleeding, Thrombosis and Vascular Biology: Vol. 4 No. s1 (2025)
- CS05 | Joint ultrasound follow-up in pediatric patients with haemophilia: a 12-year prospective single-center experience , Bleeding, Thrombosis and Vascular Biology: Vol. 4 No. s1 (2025)
- PO05 | Intensive FVIII replacement in haemophilia patients with hypertrophic synovium: a randomized study , Bleeding, Thrombosis and Vascular Biology: Vol. 4 No. s1 (2025)
- PO48 | Thrombotic risk evaluation and thrombophilia testing in β-thalassemia patients: a retrospective cohort analysis from a reference regional center , Bleeding, Thrombosis and Vascular Biology: Vol. 4 No. s1 (2025)
- PO10 | Clinical and laboratory features of long-Covid syndrome: a cross-sectional study of 1,337 Covid-19 survivors , Bleeding, Thrombosis and Vascular Biology: Vol. 4 No. s1 (2025)
- Betül Ünlü, Neha Joshi, Jamie M. O'Sullivan, Endothelial cell dysfunction in cancer: a not-so-innocent bystander , Bleeding, Thrombosis and Vascular Biology: Vol. 3 No. s1 (2024)
You may also start an advanced similarity search for this article.
Most read articles by the same author(s)
- Bianca Clerici, Mariangela Scavone, Gian Marco Podda, Recent advances in classic heparin-induced thrombocytopenia (HIT), autoimmune HIT, spontaneous HIT, and vaccine-induced immune thrombotic thrombocytopenia , Bleeding, Thrombosis and Vascular Biology: Vol. 3 No. 2 (2024)
- Marco Cattaneo, Guided antiplatelet therapy in patients undergoing percutaneous coronary intervention , Bleeding, Thrombosis and Vascular Biology: Vol. 2 No. 2 (2023)
