Colorectal carcinoma (CRC)
Time to results delivery
3-10 working days*
MEthod
Sample Collection Center
sample type
Blood draw
(2x10 ml)
Early detected CRC cancer can be cured
Over 67% of early diagnosed patients can successfully be cured – Recognize it in time!
Sensitive liquid biopsy based screening test detecting low frequency variants from blood samples with limited yield. The test helps to detect Colorectal Carcinoma before it develops to advanced stages.
More than 2/3 of early detected CRC cancer can be cured.
When should I screen?
- You are 40+
- You have got CRC in your family history
- You have got inflammatory bowel disease (crohn, ulcerative colitis)
- You experienced blood in your stool
- You loose weight from unknown reasons
- You have persistent pain or cramps in abdomen
- You have uncomfortable feeling in abdomen
Obesity
Family history / genetics
smoking & alcohol
low physical activity
Possibly associated diseases :
- Inflammatory bowel disease (Ulcerative colitis, Crohn's disease)
How does it work?
The rectum is the passageway that connects the colon to the anus.General golden recommendation is to undergo preventive CRC screening under the age of 40 and continue periodically. The most widespread type of preventive examination is a colonoscopic examination, which is, however, often ignored by “patients” because it is an unpleasant procedure. As a result many people come for screening only when feeling certain symptoms, that are usually typical for advanced phases of the disease. Here we can only use our main motto: “Recognize it until is time.”
Genetic test - detailed description
Examined DNA fragments - click on icon for detailed information
Results & How to understand the test results?
- In the genes that were analyzed, no variants known to increase cancer risk were found. Your medical doctor should evaluate your risk based on your personal and family medical history.
- A variant has been identified that may increase the risk for certain forms of cancer. You should discuss your results with your medical doctor and continue to adhere to his recommendations. There may be implications for cancer treatment in some instances.
- A variant(s) has/ve been identified, but there is insufficient evidence to determine if it increases cancer risk or affects treatment decisions. The status of a fragment of Uncertain Significance (VUS) may alter as research advances. It must be judged based on more aspects and test results. Your medical doctor should evaluate your risk based on your personal and family history.
What is Colorectal cancer?
General golden recommendation is to undergo preventive CRC screening under the age of 40 and continue periodically. The most widespread type of preventive examination is a colonoscopic examination, which is, however, often ignored by “patients” because it is an unpleasant procedure. As a result many people come for screening only when feeling certain symptoms, that are usually typical for advanced phases of the disease. Here we can only use our main motto: “Recognize it in time.”
Why to buy our genetic / genomic screening solution
1. We save you time
You don't need any reccomendation. Ones you decide to take the test, we are not asking why.
2. Online results
You will receive the results by email and you may also benefit from free access to Lomina Health-care Portal.
3. Discretion & Security
Privacy is our main objective, whatever test you take your personal data are 100% safe with us.
4. Early detection matters
Positive patients receive follow up recommendation and professional consultancy can also be ordered.
The test can be performer anytime, but usually it is recommended at the age of 40+ as an early detection method of colorectal cancer. As with many other cancers, an early detection enables very efficient treatment and recovery. The later the disease is detected, the more complicated the treatment is.
Testimonials
Jane Doe
Codetic
John Doe
Codetic
References
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Frequently asked questions
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What is genetic diagnosis?
Genetic diagnosis identifies genetic mutations causing medical conditions. It involves analyzing DNA for variations linked to disorders or increased disease risk. This informs treatment, prevention, and family planning decisions, and detects conditions earlier for better outcomes.