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How does it help me?

Verifi® Prenatal Test

Predicts the most common chromosomal abnormalities.





Predicts the most common chromosomal abnormalities.

Verifi®


There are some tests that require multiple extractions and are at high risk of false results, while the most accurate diagnostic methods such as amniocentesis have high risks to the health of pregnant and for the fetus.

Knowing all these chromosomal characteristics will allow, if the screening test is positive, get ahead and with your doctor to take the most appropriate decisions depending on each case.

Verifi® has a rejection rate of 0.1%, representing the lowest in the market, meaning that 99.9% of cases obtained results. For this, Illumina uses advanced techniques to analyze DNA fragments into the whole genome, creating an advantage over other methodologies that analyze only specific genes. This is clinically relevant considering a false positive rate not only has a negative impact on the patient but at the same time affects the parameters of sensitivity and specificity of the test. With Verifi®, the clinical impact of false positives are reduced to a minimum.

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Is the Verifi® prenatal test right for me?

Verifi® can be made to any pregnant woman who interested to know if her pregnancy, presents a chromosomal alteration, without the need to undergo invasive procedures. Especially it recommended that it made those pregnant with any of the following categories:

  • High risk due to maternal age (35 years or older at time of delivery).
  • Prenatal ultrasound showing specific changes to the baby’s growth and/or development.
  • Abnormal or positive triple test results during the first or second quarter.
  • Personal or family history of chromosomal disorders.

Why Verifi®?

There are some tests that require multiple extractions and are at high risk of false results, while the most accurate diagnostic methods such as amniocentesis have high risks to the health of pregnant and for the fetus.

Knowing all these chromosomal characteristics will allow, if the screening test is positive, get ahead and with your doctor to take the most appropriate decisions depending on each case.

Verifi® has a rejection rate of 0.1%, representing the lowest in the market, meaning that 99.9% of cases obtained results. For this, Illumina uses advanced techniques to analyze DNA fragments into the whole genome, creating an advantage over other methodologies that analyze only specific genes. This is clinically relevant considering a false positive rate not only has a negative impact on the patient but at the same time affects the parameters of sensitivity and specificity of the test. With Verifi®, the clinical impact of false positives are reduced to a minimum.

Verifi® predicts the most common chromosomal abnormalities such as:

  • Down syndrome (trisomy 21)
  • Edwards syndrome (trisomy 18)
  • Patau syndrome (trisomy 13)
  • Turner syndrome (Monosomy X)
  • Klinefelter syndrome (XXY)
  • Jacob syndrome (XYY)
  • Triple x syndrome (XXX)

Furthermore, not only can recognize if there are a problem in the number of chromosomes but also in the structure of genes, identifying identify Microdeletions (loss of part of a chromosome material) more frequent as:

  • DiGeorge syndrome
  • Angelman syndrome
  • PraderWilli syndrome
  • WolfHirschhorn syndrome
  • Criduchat syndrome

How quickly will I get my results?

Your physician will receive your results in 10 business days, and he will have professional advice to interpret the results.

Verifi® main objective is preservation of fetal and maternal health, providing a noninvasive test that allows early identification of fetal chromosomal abnormalities, through next generation technology.


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Verifi®


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Illumina

Illumina are committed to providing solutions and different options to improve the people’s health. From the beginning their products allowed researchers to explore the DNA to a new level, helping to create the first map of genetic variations associated with health, disease and response to certain treatments.

The goal is to apply innovative technologies to the analysis of genetic variations, making possible studies that were not even imaginable a few years ago. The idea is always to get adequate and accessible solutions to patient’s needs .

Illumina is a global leader in genetics, an industry where technology is intersecting with biology. At the most fundamental level it seeks to enable patients to understand the genetic variations, seeking to make it solutions as simple and accessible as possible without losing their high level of confidence. As a result, findings that were unimaginable a few years ago are routine today and allow better treatments for patients.

Nowadays sequence can describe to an unprecedented scale. This makes a lot deeper understanding of genetics as never before starting to unlock the true power of the genome. These advances will bring a fundamental change in health care, leading medicine to an increasingly more preventive and accurate place.

SouthGenetics

SouthGenetics es una empresa líder en el área de la comercialización de servicios de biotecnología. Nuestra misión es proveer a médicos y pacientes un rápido acceso a los servicios de diagnósticos genómicos de alta complejidad. A través de acuerdos estratégicos con los principales laboratorios del mundo en cada área brindamos servicios diagnósticos con foco en oncogenómica y en desórdenes cromosómicos.

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