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Our Services > CGT

CGT: Carrier Genetic Test

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

  • Overview
  • 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 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%.

3 CGT Options according to your needs

CGT Exome

Whole exome compatible with most carrier platforms in the market.

CGTPlus

Based on the recommendation of medical societies.

CGT Essential

Cost-effective solution.

More Information about CGT
Features
  • Benefits
  • Indications

Why use CGT?

  • Study up to 1590 genes linked to 1600 genetic disorders
  • Genetic counseling for patients
  • Availability of a specific unit for gametes donor programs
  • 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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Prevents the transmission of single gene disorders

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