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IGENOMIX – With science on your sideIGENOMIX – With science on your side
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Genetic Solutions > POC

POC Products of Conception

Studies fetal tissue from a lost pregnancy to check whether the miscarriage was the result of chromosomal aneuploidy

  • Technical Overview
  • Documentation
  • Scientific evidence
  • I’m not a health specialist

25% of all recognized pregnancies are miscarriages

50% of first trimester pregnancy losses are due to chromosomal abnormalities

60% of first trimester pregnancy losses are due to chromosomal abnormalities after ART

Reliable results are obtained in 99% of cases

Are you interested?

Request information Or email us at infousa@igenomix.com
Overview
  • POC
  • Benefits
  • Indications

What is POC?

The POC test analyzes fetal tissues from a miscarriage to determine if the loss was the result of a chromosomal aneuploidy.  

This test can provide you with important information about the possible causes of your patient’s miscarriage and help you determine the next steps for their fertility treatment.   

What is the procedure?

Why use POC test?

The genetic study of fetal tissue is a valuable tool to determine the cause of the miscarriage, which enables appropriate reproductive counseling for the couple.

  • Results are obtained in 99% of cases.
  • Results will be available in 7 days as cell culture is not required.
  • 24 chromosomes are screened to identify the reason for miscarriage.
  • Can be performed on twin pregnancies.
  • Our test discriminates between maternal and fetal tissue using DNA fingerprinting (STR Technology).
  • NGS has higher resolution than a conventional karyotype.

Who should use POC test?

  • It is recommended for all couples who have suffered a miscarriage but is essential for couples who have experienced recurring spontaneous abortions or those undergoing assisted reproduction treatments.

Test Limitations

  • This technique does not detect balanced structural chromosomal abnormalities and may not detect: low-level mosaic aneuploidy, triploid/tetraploid chromosomes, uniparental disomy, deletions or duplications under 10 Mb.
Documentation
  • Specialists

Clinical Sheets

Download
Scientific evidence

Relevant studies:

Campos-Galindo I, et al. J Assist Reprod Genet 2012; 32:839-48

Martínez MC, et al. Fertil Steril 2010;93:289-92.

If you´re a little lost with this technical information...

Can we help you?

I’m not a health specialist

Igenomix and fertility

We work to make a world in which infertility is no longer an impossible barrier. Together with clinics and fertility doctors worldwide we investigate human reproduction to change the lives of couples who are trying to conceive.

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Igenomix is not affiliated with any news outlet or publication identified above. News coverage does not constitute an endorsement of Igenomix or its products.

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  • We guide you
    • Fertility
  • Reproductive Health
    • Specialists
      • ERA
      • EndomeTRIO
      • EMMA
      • ALICE
      • COVID-19 PCR
      • PGT-A + ERA Synchrony
      • PGT-A
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      • PGT-M
      • SAT
      • POC
      • Oncodona
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