Health Check
Types Of HPV Infections- Low Risk & High Risk
4 mins | November 25, 2022
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Order Your Test Online
• Order your Double Marker test online.
• Upload your recent ultrasonography (USG) report to confirm the order.
Collect Sample
• Schedule maternal blood sample collection by a trained paramedic at a registered collection centre or at home.
• For measurement of probability of the chromosomal abnormalities, nuchal translucency scan and nasal bone scan is required, which will be provided by your healthcare provider. You will have to upload this scan report while ordering your test.
Receive Digital Results
Within days, usually 36 hours, you’ll receive your digital results on your personalised dashboard.
Follow Up
Schedule a virtual consultation with our genetic counselors to understand your Double Marker test results better.
Customised Dashboard Experience:
Along with an interactive, user-friendly experience, we also offer you the complete screening test insight in the form of smart reports.
SMART Reports:
Empowering you with the right information, our SMART reports are-
Personalised Recommendations
We want you to understand the logic and science behind what we do. So, your report is not just about numbers but is crafted in a way to help you visualise and comprehend the why, what, how, as well as the next steps of your healthcare journey!
Certifications & Accreditations
As per NABL & CAP certification, our labs have high
testing standards & submit to regular inspections. We participate in external quality assurance
program by CAP & UK-NEQAS*. We also regularly monitor & update medians & algorithms as per FMF
(UK) guidelines. We adhere to ISTD updates to maintain processing quality.
*United Kingdom National External Quality Assessment Service
Trusted by Healthcare Experts
We are India’s largest provider for innovative and comprehensive preconception, prenatal and newborn diagnostic services.
Privacy & Confidentiality
Your privacy is our priority. We use state-of-the-art technology to ensure your data is stored securely, and under no circumstance do we ever sell your data.
Seamless Paramedic & Customer Support
With an expert team of well-trained paramedics across India, you can be rest assured to get a smooth testing experience for all your and your family’s needs.
Advanced Software & Testing Platforms
Our advanced testing platforms and softwares comply with FMF Good Laboratory Guidelines and follow satisfactory laboratory Standard Operating Procedures (SOP) for prenatal screening. Learn More
PNDT-Registered by Govt to Conduct Prenatal Diagnostic Tests
As per our registration under Prenatal Diagnostic Techniques (regulation and prevention of misuse) act, 1994, LifeCell’s labs perform preconception & prenatal tests in a fair manner, & do not conduct prohibited sex determination tests or disclose the baby’s gender as per Government rules.
Wish To Know More?
This test analyzes maternal blood in the first trimester of pregnancy to detect most common chromosomal abnormalities in the fetus.
The test results are accurate when it is done in the first trimester of the pregnancy between the 10th-13th week.
No, the ideal time for performing the test is between 10 th-13 th weeks of pregnancy.
The cost of the Double Marker test depends on the Diagnostic center you opt for. However, the average cost of the test usually isn’t expensive and is quite reasonable.
The Double Marker test uses maternal blood samples, ultrasound & a Nuchal Translucency (NT) scan of the fetus.
The Double Marker test is a non-fasting, simple blood test. You can eat food or drink fluids as usual before and after the test.
You will receive your digital Double Marker test reports within 36 hours.
High risk factors for testing positive include women over the age of 35, family history of Down's Syndrome, or adverse obstetric history.
If the results are positive for the Double Marker test, then the doctor will recommend a few more tests to further confirm the probability of the baby being born with a genetic disorder.
If the Double Marker test results are negative/low risk, it means that the risk of your baby having any chromosomal or neurological defects is less.