The CGT is a genetic family planning test that allows you to evaluate the risk of having a child with a genetic disease. The test will determine if the parents are carriers or less of one or more genetic mutations.
THE FERTILE GROUP CLINIC TREATMENTS
Carrier Genetic Test (CGT)
The Fertile Group offers advanced genetic diagnostic techniques to advise patients on their reproductive future, reducing the risk of genetic disease in their offspring even before taking the first step.
The CGT is a genetic family planning test that allows you to evaluate the risk of having a child with a genetic disease.
Carrier Genetic Test
The Carrier Genetic Test (CGT or Genetic Carrier Screening) is a test that analyzes the genes of the couple to detect possible alterations or mutations in them Once the results of both members of the couple are obtained, our specialists cross their information thanks to a powerful and secure computer system, which allows us to see the coincidences and, therefore, also the incompatibilities at chromosomal level.
Our specialists are firmly committed to the health of both mothers and babies born through The Fertile Group’s advanced assisted reproduction techniques.
Por este motivo, recomiendan efectuar el PGT-A en los siguientes casos:
01
Genetic diseases cannot be cured, but we can prevent them.
02
Anyone can be, without knowing it, a carrier of one or more mutations.
03
The carriers are usually healthy people
The carriers are usually healthy people, but when both parents are carriers of the same genetic mutation, their union could lead to a child affected by that specific disease.
04
This analysis allows our patients to identify genetic diseases
This analysis allows our patients to identify genetic diseases of poor prognosis in children, such as cystic fibrosis, fragile X syndrome or spinal muscular atrophy, among others.
Although we all have alterations in our genes, with CGT, the carrier genetic compatibility test, future parents will be able to know if they could cause an eventual disease to their children or not.
The Fertile Group recommends this test in this following cases:
01
Before attempting natural pregnancy methods, any couple wishing to conceive can assess the risk of transmitting potential diseases to their child.
02
Before undergoing assisted reproduction treatment, it is advisable to assess the risk of transmission to determine the best treatment approach for the couple.
03
It has a sensitivity close to 100% for detecting Down syndrome and poses no risk to the mother or the baby.
04
It is a non-invasive prenatal test that allows detection of the most common chromosomal abnormalities, primarily Down syndrome, starting from the 10th week of pregnancy.
Goal
Ensuring healthy offspring, avoiding the transmission of diseases to future generations.
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