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CGT

CGT: Carrier Genetic Test

Genetic disorders can’t be cured, but they can be prevented

  • Overview
  • CGT Gene List
  • Features
  • How does it work?
  • I’m a health specialist

82% of individuals
are carriers of at least one condition

Every person
has an average of 2 genetic mutations

5% of couples
carry the same mutation

Inherited disorders represent
20% of the causes of infant mortality in developed countries

Overview

What are genetic diseases?

  • Genetic diseases are caused by mutations (changes to our genes).
  • Mutations can be present in DNA without affecting the individual, thus that individual would be a carrier of the condition.
  • 82% of individuals are carriers of at least one condition.

(*) Kingsmore S. PLOS Currents Evidence on Genomic Tests. 2012 May 2. Edition 1. doi: 10.1371/4f9877ab8ffa9.

What is Carrier Genetic Test (CGT)?

  • CGT is an important genetic test when planning a family, because it helps to determine the risk of having a child with a genetic disease.
  • CGT determines whether you and your partner or donor are carriers of single-gene recessive conditions: if you both carry the same mutation, the probability of having a sick child is 25%.

Our New Universal approach to expanded carrier screening using Whole Exome Sequencing

CGT Plus

Examines a larger list of genes associated with over 500 genetic conditions. This panel-based test is recommended when both individuals in a reproductive couple are seeking CGT to find out if they might be carriers of the same genetic condition(s), or when individuals are looking to donate eggs/sperm.

CGT Mirror

A test that facilitates “mirroring” a carrier screening test performed by a different genetic testing laboratory to ensure that the two panels include the same genes. Panels can vary between laboratories and over time. CGT Mirror can be considered when one member of the reproductive couple has already had carrier screening and the other member wishes to have a similar panel of genes tested.

CGT Sequential

May be considered when one individual in a reproductive couple (one partner or a sperm/egg donor) is a known carrier of one or more autosomal recessive genetic conditions. CGT Sequential can be ordered for the reproductive partner and includes analysis of the gene(s) of interest. The optional analysis of X-linked conditions is available for biologically female patients.

More Information about genes and mutations
Features
  • Benefits
  • Indications

Why use our CS Exome Based?

  • Allows for testing of all known recessive conditions
  • Genetic counseling for patients
  • Availability of a specific unit for gametes donor programs
  • Maximizes IVF applications, matching possible with all genetic lab tests in the market.
  • CGT is based on next generation sequencing (NGS) and it’s clinically validated

Is CGT for you?

CGT is recommended if:
  • You want to know the risk of transmitting possible disorders to your future children, regardless of your reproductive plans.
  • You’re going to start assisted reproduction treatment.
  • You’re staring a treatment involving a sperm or egg donor.
How does it work?

BROCHURE

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Other services

PGT-M

Prevents the transmission of single gene disorders More information

PGT-A + ERA Synchrony

The best embryo at the right time More information

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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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  • PATIENT JOURNEY
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  • Reproductive Health
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      • EMMA
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      • CGT
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      • PGT-A
      • PGT-SR
      • Family Balancing
      • EMBRACE
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