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CGT: Carrier Genetic Test

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

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 Exome

Oremium expanded Panel compatible with most carrier platforms in the market.

CGTPlus

Based on the recommendation of medical societies.

CGT Bank

An exclusive panel for Gamete Donors

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?

Other services

PGT-M

(単一遺伝子疾患の着床前遺伝検査)

PGT-M検査は、遺伝性疾患を遺伝させるリスクのあるカップルをサポートします。この遺伝子検査は、将来生まれてくる赤ちゃんへの遺伝性疾患の遺伝を防ぎ、健康な妊娠を目指します。

詳しくはこちら

NACE検査

非侵襲性の出生前検査

Nace検査は、簡単な血液検査でダウン症などの異常を調べることができます。
胎児や母体を危険にさらすことなく、赤ちゃんの染色体数を調べるため、どの妊婦さんにも実施可能な検査です。

詳しくはこちら

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

What are genetic diseases?

What is Carrier Genetic Test (CGT)?

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

CGT Exome

CGTPlus

CGT Bank

Why use our CS Exome Based?

Is CGT for you?

BROCHURE

PGT-M

NACE検査

CGT: Carrier Genetic Test

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

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

What are genetic diseases?

What is Carrier Genetic Test (CGT)?

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

CGT Exome

CGTPlus

CGT Bank

Why use our CS Exome Based?

Is CGT for you?

BROCHURE

Other services

PGT-M

NACE検査

Igenomix is in the media

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