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MaterniT GENOME

MaterniT GENOME gets more information about the fetus’ chromosomes than any other Noninvasive Test.





FIND NOW THE TEST the MaterniT GENOME Test

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Is the only Noninvasive Prenatal Test analyzing all chromosomes.

MaterniT GENOME


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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.

Do you want to know more about the MaterniT GENOME Test?

KNOW MORE ABOUT THIS TEST IN YOUR COUNTRY

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

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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 .

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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