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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
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Subjects:
Genetics & Heredity
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Update Date:
24 Dec 2020
Table of Contents
1. Introduction
Individuals with mild protein C deficiency are at risk of a type of blood clot known as a deep vein thrombosis (DVT). These clots occur in the deep veins of the arms or legs, away from the surface of the skin. A DVT can travel through the bloodstream and lodge in the lungs, causing a life-threatening blockage of blood flow known as a pulmonary embolism (PE). While most people with mild protein C deficiency never develop abnormal blood clots, certain factors can add to the risk of their development. These factors include increased age, surgery, inactivity, or pregnancy. Having another inherited disorder of blood clotting in addition to protein C deficiency can also influence the risk of abnormal blood clotting.
In severe cases of protein C deficiency, infants develop a life-threatening blood clotting disorder called purpura fulminans soon after birth. Purpura fulminans is characterized by the formation of blood clots in the small blood vessels throughout the body. These blood clots block normal blood flow and can lead to localized death of body tissue (necrosis). Widespread blood clotting uses up all available blood clotting proteins. As a result, abnormal bleeding occurs in various parts of the body, which can cause large, purple patches on the skin. Individuals who survive the newborn period may experience recurrent episodes of purpura fulminans.
2. Frequency
Mild protein C deficiency affects approximately 1 in 500 individuals. Severe protein C deficiency is rare and occurs in an estimated 1 in 4 million newborns.
3. Causes
Protein C deficiency is caused by mutations in the PROC gene. This gene provides instructions for making protein C, which is found in the bloodstream and is important for controlling blood clotting. Protein C blocks the activity of (inactivates) certain proteins that promote blood clotting.
Most of the mutations that cause protein C deficiency change single protein building blocks (amino acids) in protein C, which disrupts its ability to control blood clotting. Individuals with this condition do not have enough functional protein C to inactivate clotting proteins, which results in the increased risk of developing abnormal blood clots. Protein C deficiency can be divided into type I and type II based on how mutations in the PROC gene affect protein C. Type I is caused by PROC gene mutations that result in reduced levels of protein C, while type II is caused by PROC gene mutations that result in the production of an altered protein C with reduced activity. Both types of mutations can be associated with mild or severe protein C deficiency; the severity is determined by the number of PROC gene mutations an individual has.
4. Inheritance
Protein C deficiency is inherited in an autosomal dominant pattern, which means one altered copy of the PROC gene in each cell is sufficient to cause mild protein C deficiency. Individuals who inherit two altered copies of this gene in each cell have severe protein C deficiency.
5. Other Names for This Condition
- hereditary thrombophilia due to protein C deficiency
- PROC deficiency
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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Xu, R. Protein C Deficiency. Encyclopedia. Available online: https://encyclopedia.pub/entry/5494 (accessed on 28 September 2023).
Xu R. Protein C Deficiency. Encyclopedia. Available at: https://encyclopedia.pub/entry/5494. Accessed September 28, 2023.
Xu, Rita. "Protein C Deficiency" Encyclopedia, https://encyclopedia.pub/entry/5494 (accessed September 28, 2023).
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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