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CLINICAL GENETICS

NIPT Plus – Non-Invasive Prenatal Test Plus

A Safer Way to Learn About Your Baby’s Health.

Starting from just 10 weeks of pregnancy, the NIPT Plus screens for Down syndrome (Trisomy 21), Edwards syndrome (Trisomy 18), Patau syndrome (Trisomy 13) and provides accurate gender determination. But it doesn’t stop there — it also checks for sex chromosome aneuploidies, additional autosomal aneuploidies, as well as microdeletion and duplication syndromes. And the best part? All of this is done through a simple blood draw from the mother, with no risk to the baby.

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What is NIPT Plus?

NIPT Plus is an advanced version of the Non‑Invasive Prenatal Test (NIPT) designed to give expecting parents the most comprehensive view of their baby’s chromosomal health.

Building on the NIPT Basic, which screens for the core conditions, NIPT Plus expands coverage to include:

6 Sex Chromosome Aneuploidies (SCAs):

  • Turner syndrome (XO)
  • Triple X (XXX)
  • XYY
  • Mosaic variations (XO+XY, XXX+XY)

 

19 additional autosomal aneuploidies beyond the common trisomies.

Over 60 microdeletions and duplications, including:

  • Jacobsen syndrome
  • Split‑hand/foot malformation
  • DiGeorge syndrome 2
  • Holoprosencephaly 6

 

This expanded screening is ideal for parents who want greater reassurance and peace of mind, offering insights into both common and rare chromosomal conditions.

And the best part? All of this is achieved through a simple blood draw from the mother, with no risk to the baby.

This test is designed for:

  • Expectant parents wanting early and greater reassurance
  • Families with history of chromosomal conditions
  • Parents seeking a safe alternative to amniocentesis or CVS
  • Parents wanting a comprehensive view of their baby’s chromosomal health

Why This Test Matters

For Patients & Families

  • Identify inherited cancer risks early.

  • Take preventive steps such as enhanced screening or lifestyle changes.

  • Share results with relatives for family‑wide health planning.

For Providers

  • Improve patient care with genetic insights.

  • Guide referrals, screening protocols, and preventive interventions.

  • Support cascade testing for at‑risk family members.

For Proactive Consumers

  • Even without a family history, you may carry mutations that increase cancer risk.

  • Knowledge empowers you to take control of your health.

Conditions screened

Trisomy 21 (Down syndrome)

Trisomy 18 (Edwards syndrome)

Trisomy 13 (Patau syndrome)

6 Sex chromosome

Aneuploidies (SCAs) (XO/XXX/XYY/XO+XY/XXX+XY)

Other 19 autosomal

Aneuploidies

60 Microdeletion/ Duplication Syndromes

Sex identification

Fetal fraction estimation

What you will learn from this test

  • Early risk assessment for trisomies
  • Early risk assessment for all chromosomal aneuploidies
  • Early risk assessment for microdeletions and duplications
  • Whether further testing is needed weeks before ultrasound scans
  • Your baby’s gender with high accuracy
  • Whether more invasive testing or specialist care may be needed
  • Fetal fraction percentage confirming reliability
  • Knowledge to plan ahead with confidence

Why choose NIPT?

  • Early detection : from 10 weeks
  • Non-invasive: just a maternal blood draw
  • Highly accurate: >99% for trisomies and aneuploidies
  • Fetal fraction included for quality assurance
  • Validated in African populations

How it works

Order the test online or through your provider

Provide one blood draw from the mother’s arm

Receive results within 5–7 days

Pricing

Plan with the right information.
Order Your NIPT Plus Today

NIPT – Non-Invasive Prenatal Test

₦760,000

(For Provider)

Order Test

NIPT – Non-Invasive Prenatal Test

₦800,000

(Direct-to-Consumer)

Order Test