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MaterniT GENOME

MaterniT GENOME gets more information about the fetus’ chromosomes than any other Noninvasive Test.
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Is the only Noninvasive Prenatal Test analyzing all chromosomes.

MaterniT GENOME

MaterniT GENOME is an analysis that all women who wants to get early information as possible about their pregnancy without the risks associated with invasive testing, from 10 weeks of pregnancy can perform.

MaterniT GENOME is the most complete Noninvasive Prenatal Test that exists today, able to analyze all fetal chromosomes without any risk to you or your baby.

MaterniT GENOME analyzes all chromosomes, providing the most information available at the date. It can detect 25% more chromosomal alterations present than any other non-invasive prenatal test.

Prenatal Test

MaterniT GENOME

Is the only Noninvasive Prenatal Test analyzing all chromosomes.
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WHAT MATERNIT GENOME INFORM?

MaterniT GENOME test analyzes all chromosomes, including the most common such as:

  • Trisomy 21 (Down Syndrome)
  • Trisomy 18 (Edwards Syndrome)
  • Trisomy 13 (Patau syndrome)

Sex chromosome aneuploidy:

  • Turner Syndrome
  • Jacobs Syndrome
  • Klinefelter Syndrome
  • Triple X Syndrome

Microdeletions:

  • DiGeorge Syndrome
  • PraderWilli syndrome / Angelman
  • Jacobsen Syndrome
  • LangerGiedion Syndrome
  • WolfHirschhorn syndrome
  • Syndrome Criduchat
  • Deletion Syndrome 22q11
  • Panel of losses and profits of genetic material at chromosomal level (translocations, investments and insertions)

Additionally, it provides the sex of the fetus

Sequenom

Provides the best laboratory testing services, focusing on prenatal test. Also includes MaterniT21®PLUS the leader and pioneer in the noninvasive prenatal test market for use in pregnant women at increased risk for fetal aneuploidy. As well as visibiliT .

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