Goanic Integrated Laboratory Services

How Does NIPT Work?

Small amounts of a baby’s DNA passes into the bloodstream of the mother during pregnancy. New technology allows us to analyse this DNA directly from the mother’s blood and screen for chromosomal abnormalities.

Previously, it was only possible to test for these abnormalities with highly invasive procedures that carried a risk to the pregnancy. Chorionic villus sampling (CVS) can be performed between weeks 10-12 and pregnancy, and amniocentesis performed between weeks 15–18 of pregnancy. These tests carry up to 1 in 150 or 1 in 100 chance of miscarriage respectively.

Initial screening with non-invasive prenatal testing can help to avoid this potentially unnecessary and invasive testing. There is no risk to mother or baby and NIPT provides the earliest testing available.

Call +2347068951861 for more inquiries

Click on the link below to learn more👇
https://www.centogene.com/patient/genetic-testing/non-invasive-prenatal-testing-nipt

Non-Invasive Prenatal Testing – No Risk to Mother and Baby

Want to make sure that your baby is growing and developing normally during pregnancy? CentoNIPT® – Safe and accurate prenatal testing – Offers you information about the health and development of your child from as early as the 10th week of pregnancy.

Non-invasive prenatal testing (NIPT) is a new method of testing for common chromosomal abnormalities that can occur in a developing baby. While rare, these chromosome abnormalities can have profound consequences to the life and health of you and your child and it is important to find out as soon as possible.

Call +2347068951861 to order for a test.

Click on link below to learn more👇
https://www.centogene.com/patient/genetic-testing/non-invasive-prenatal-testing-nipt

Breast Cancer is common and often treatable. But despite new treatments, breast cancer that has spread to other organs still has a high mortality rate. Several genes have been linked to a higher risk of developing breast cancer. Approximately 1 in 8 women will be diagnosed with invasive breast cancer. Breast cancer risk is associated with several factors, including gender, age, race / ethnicity, excess body weight, exposure to hormone therapy, alcohol consumption, smoking, family or personal history, and genetic predisposition, among others. One of the strongest risk factors is genetic predisposition, with mutations in accounting for 5% to 10% of all cancers.

🧬testing can help you and your doctor decide from various options for prevention, screening, and treatment for breast .

Centogene offers excellent caring services for reliable breast cancer testing; CentoBreast® has been designed to test for a wide range of genes linked to breast cancer, as well as and ovarian cancer and for the differential diagnosis of other syndromes, such as Lynch, Codwen, Peutz-Jeghers, and Li-Fraumeni syndromes.

We help you at every step of processing your request.
To order a test or inquiries call Bamiras +2347068951861

NEWBORN SCREENING

Designed to address multiple genetic conditions that may present in the newborn or first childhood period.

It allows clinicians to utilize just one single test to provide an accurate diagnosis of newborn-related diseases.

Screens newborns for all ACMG-recommended conditions and those nominated for inclusion.

10 working Days TAT

CARRIER SCREENING

The earliest step to responsible family planning, because most people can be carriers of a disease-causing change without knowing it.

Offered to individuals considering a pregnancy or in early pregnancy.

It is appropriate for individuals or couples with the following backgrounds:
1. No family history of genetic disease
2. A Known family history of genetic disease
3. High consanguinity
4. Ethnicities with high incidence of genetic diseases

Getting tested early gives future parents the opportunity to make informed decisions and review the range of options available to guide pregnancy and family planning.

Call us +2347068951861 for your screening!

What you should know about
OUR PRENATAL DIAGNOSIS:

The choice of the appropriate testing strategy and a quick response are key factors to minimize the stress.

We offers a turnaround time of ten business days for most prenatal analyses (known variants, deletion/duplication analysis, single gene sequencing) and of less than 15 business days for NGS (next generation sequencing) analyses.

In addition, our medical experts are always available for your support before, during and after the analysis.

CALL +2347068951861

NON-INVASIVE PRENATAL TESTING

Screen for any fetal chromosomal abnormalities.

Reveal genetic health of developing foetus

Test performed on a single maternal blood sample + latest NGS

Provides unparalleled quality accuracy and detection.

5 working days TAT + QA

Goanic Integrated Laboratory Services Goanic is dedicated to wide range of integrated services, as well as investing in genetic testing.

We are into genetic testing and diagnosis of rare disease.

By choosing our services, you gain access to a wide range of cutting-edge genetic and multiomic testing options. We understand that a timely and accurate diagnosis is crucial for patients and physicians, that's why we offer a comprehensive diagnostic solutions in global clinical network, and deep medical expertise as powered by our International Partner Centogene GmbH, Germany.

SCIENCE LABORATORY EQUIPMENT AND CONSULTANCY SERVICES (SLEC)
Are u an under graduate physics student or physics production STUDENT or even an engineering student ....then SLEC is for you.
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Visit SLEC laboratory at uniport park or call 08036677183 or jxt inbox me.