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| Version | Summary | Created by | Modification | Content Size | Created at | Operation |
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| 1 | Rita Xu | + 525 word(s) | 525 | 2020-12-15 07:36:07 |
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Xu, R. Protein C Deficiency. Encyclopedia. Available online: https://encyclopedia.pub/entry/5494 (accessed on 21 September 2026).
Xu R. Protein C Deficiency. Encyclopedia. Available at: https://encyclopedia.pub/entry/5494. Accessed September 21, 2026.
Xu, Rita. "Protein C Deficiency" Encyclopedia, https://encyclopedia.pub/entry/5494 (accessed September 21, 2026).
Xu, R. (2020, December 24). Protein C Deficiency. In Encyclopedia. https://encyclopedia.pub/entry/5494
Xu, Rita. "Protein C Deficiency." Encyclopedia. Web. 24 December, 2020.
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Protein C deficiency is a disorder that increases the risk of developing abnormal blood clots; the condition can be mild or severe.
genetic conditions
References
- Brouwer JL, Lijfering WM, Ten Kate MK, Kluin-Nelemans HC, Veeger NJ, van derMeer J. High long-term absolute risk of recurrent venous thromboembolism inpatients with hereditary deficiencies of protein S, protein C or antithrombin.Thromb Haemost. 2009 Jan;101(1):93-9.
- Cafolla A, D'Andrea G, Baldacci E, Margaglione M, Mazzucconi MG, Foà R.Hereditary protein C deficiency and thrombosis risk: genotype and phenotyperelation in a large Italian family. Eur J Haematol. 2012 Apr;88(4):336-9. doi:10.1111/j.1600-0609.2011.01742.x.
- Goldenberg NA, Manco-Johnson MJ. Protein C deficiency. Haemophilia. 2008Nov;14(6):1214-21. doi: 10.1111/j.1365-2516.2008.01838.x.
- Knoebl PN. Severe congenital protein C deficiency: the use of protein Cconcentrates (human) as replacement therapy for life-threatening blood-clottingcomplications. Biologics. 2008 Jun;2(2):285-96.
- Mahmoodi BK, Brouwer JL, Ten Kate MK, Lijfering WM, Veeger NJ, Mulder AB,Kluin-Nelemans HC, Van Der Meer J. A prospective cohort study on the absoluterisks of venous thromboembolism and predictive value of screening asymptomaticrelatives of patients with hereditary deficiencies of protein S, protein C orantithrombin. J Thromb Haemost. 2010 Jun;8(6):1193-200. doi:10.1111/j.1538-7836.2010.03840.x.
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