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PGD

Preimplantation Genetic Diagnosis

Now known as PGT-M (Preimplantation Genetic Testing for Monogenic/Single Gene Defects)

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Overview

  • For couples with a family history of monogenic diseases such as cystic fibrosis, fragile X syndrome, Huntington's Disease, etc.
  • The diagnosis is performed on the embryo as part of an assisted reproduction treatment, before it is transferred into the uterus.
  • Through analysis of the embryos, it is possible to select those that are free from the disorder.

 

Overview

Benefits

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Higher chance of a healthy baby

It maximizes the chances of having a baby free from the disease for couples who have a high genetic risk.

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Possibility of PGD (PGT-M) + PGS (PGT-A)

We can perform PGD (PGT-M) and PGS (PGT-A) for screening of aneuploidies in the same biopsy.

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We can perform PGD (PGT-M) for most monogenic disorders
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The PGD (PGT-M) test is already developed for more than 300 diseases

Methodology

Methodology
Technology

Technology

Igenomix uses state of the art technology for PGD (PGT-M).

  • Igenomix uses a multiple detection approach to ensure the most reliable results.
  • Using direct detection, PCR is used to detect the specific disease causing mutation.
  • Using indirect detection, linkage analysis uses PCR to detect informative STR markers that are linked to the disease-causing gene.
  • Our multiple detection strategy minimizes the chances of no results or misdiagnosis due to allele drop out (ADO).
  • With our technology, our PGT-M testing is 98-99% accurate.

Our results

We are proud to deliver high quality results for every test, every day. Our experts are professional, reliable and approachable and are available to help guide both professionals and patients throughout the entire process.

300

DIFFERENT DISEASES

2,5 K

CYCLES

20+

YEARS EXPERIENCE
IN GENETICS

98%

ACCURATE

Become our provider

We will help you get started quickly and efficiently

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