Cystic fibrosis-CFTR(32 mutations) with maternal cell contamination analysis in Modasa
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Cystic fibrosis-CFTR(32 mutations) with maternal cell contamination analysis1
FAQ
How does this test differ from exonic or full gene sequencing?
This panel specifically targets 32 known CF mutations rather than scanning the entire gene, making it a quicker and more cost-effective option for known mutation detection.
What is maternal cell contamination, and why is it important to check for it?
Maternal cell contamination refers to the presence of the mother's DNA in the fetal sample, which can lead to inaccurate results. Checking for it is crucial to ensure the sample represents the fetus’s DNA.
Can this test detect all types of cystic fibrosis mutations?
While this test covers the most common 32 mutations, there are many other mutations it may not detect. For a comprehensive analysis, full gene sequencing might be recommended.
Is the test suitable for prenatal screening?
Yes, it's suitable for prenatal screening, especially with maternal cell contamination analysis, to ensure the fetal sample's purity.
What other packages does Sterling Accuris offer?
Sterling Accuris offers a range of packages including Senior citizen (male and female) package, healthy heart profile, diabetes profile, vitamin profile, covid immunity package and much more. Visit our website to learn more about these packages.
What makes Sterling Accuris a better pathology lab than others?
For us, precision care, safe sample collection, timely delivery of reports, and precise reporting of patient results while adhering to health and safety precautions are the cornerstone of our success.
Do you provide home visit/collection service?
Yes. We do provide home collection services at your doorstep.
Please go ahead and book your visit today from our top menu options in this website / chat or do call us on 812 813 0000.
How long does it take to receive test results?
Though most tests are completed and reported within about 24 hours of receiving the sample for testing, certain tests take several days to weeks.
Your soft copy will be sent on registered email id and Whatsapp. Also, you will receive SMS with link to download your report. Also, your report is available on our website / app.
To know the status of the report, you can call our customer care team on 812 813 0000.
Is there any preparation or precautions for patient before tests or body checkup?
Fasting maybe required in case of a few tests to ensure accurate results.
In general, it is also advisable to abstain from alcohol and heavy diet at least for 24 hours before any health test. You can see the requirement for each test on the product page on our website / app.
Cystic Fibrosis-CFTR (32 Mutations) with Maternal Cell Contamination Analysis in Modasa
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Sterling Accuris Diagnostics expands its genetic testing menu with the Cystic Fibrosis-CFTR (32 Mutations) panel in Modasa, accompanied by maternal cell contamination (MCC) analysis. This enhanced diagnostic tool not only screens for the most common CFTR gene mutations but also ensures the integrity of the sample with an additional MCC check.
Distinguishing Features of the CFTR (32 Mutations) Panel with MCC Analysis
This tailored test panel is designed to detect 32 well-characterized mutations in the CFTR gene, which are commonly associated with cystic fibrosis. By incorporating maternal cell contamination analysis, the accuracy of the test is significantly increased, as it confirms that the fetal DNA samples are free from maternal DNA, which can lead to false results.
Benefits of the CFTR (32 Mutations) Panel with MCC Analysis
- Targeted Mutation Detection: Specifically identifies the 32 most prevalent CFTR mutations, providing a focused genetic outlook.
- Enhanced Accuracy: Maternal cell contamination analysis validates that the samples are uncontaminated, offering a higher degree of result reliability.
- Informed Clinical Decisions: Accurate identification of mutations aids in personalised treatment planning and genetic counselling.
Ideal Candidates for the Test
- Expectant mothers undergoing prenatal testing for cystic fibrosis.
- Families with a history of cystic fibrosis seek comprehensive genetic analysis.
- Individuals with clinical symptoms that warrant detailed CFTR mutation investigation.
Cystic Fibrosis-CFTR (32 Mutations) with Maternal Cell Contamination Analysis in Modasa may use:
- Polymerase Chain Reaction (PCR) to amplify specific segments of DNA, allowing for the detection of specific mutations within the CFTR gene.
- Next-Generation Sequencing (NGS) to provide a comprehensive analysis of the gene.
- Sanger sequencing to read the order of DNA bases in a gene, one piece at a time.
In addition, the maternal cell contamination analysis is performed using short tandem repeat (STR) markers, which are highly effective in distinguishing between fetal and maternal DNA.
Essentials of the CFTR (32 Mutations) Panel with MCC Analysis
- Preparation: No fasting is required; simply follow your doctor's instructions.
- Suitability: Appropriate for individuals of any age, including infants, for early detection.
- Sample Requirement: A blood sample in EDTA is collected.
Sterling Accuris Diagnostics ensures meticulous analysis and confidentiality in all genetic testing procedures. Trust us for comprehensive cystic fibrosis testing with our Cystic Fibrosis-CFTR (32 Mutations) with Maternal Cell Contamination Analysis in Modasa. Schedule your home visit appointment today for peace of mind and a clear path forward in CF management.
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