Reproductive Genetics

Preconception genetic testing

Pre-Implantation Genetic Screening (PGS) involves a process of screening of embryos in the course of In Vitro Fertilization (IVF). This helps to identify abnormalities in the chromosomes occurring due to aneuploidy. The main reason for recurrent IVF failures and in turn pregnancy losses is the higher risk of chromosomal errors that happen at advanced maternal age. It is in this scenario, PGS helps to ascertain the best embryos thereby improving the chances of carrying out healthy pregnancies. The success rate of an IVF attempt also increases because of this. Genetic disorders can be diagnosed before implementation. Hence, the significance of this option is attributed to the fact that the only other option could very well be the medical termination of pregnancy itself. This method ensures good health for both the newly born child as well as the mother.

Studies have shown that PGS may be most beneficial for couples meeting one of the following criteria.

  • Advanced maternal age 
  • Previous IVF/ICSI Failures or Recurrent implantation failures
  • Chromosomal abnormalities like Mongolism
  • Sex chromosomal related disorders
  • Fragile X syndrome
  • Male infertility related conditions

Argenomics becomes the first centre in India to have an in-house facility for PGS i.e. screening all the 23 pairs of chromosomes using the latest Ion S5 XL Next-generation sequencing platform.

Argenomics EnsureCCS+ screens all 24 chromosomes for aneuploidy. Thus, increasing your chances of achieving a healthy pregnancy and also, decreasing your risk of miscarriage by identifying embryos with the healthy number of chromosomes.

How does PGS work?

Advantages of getting PGS testing done at ARGENOMICS

When conducted the testing at Argenomics, a full embryonic Karyotype is provided with all the 23 pair screening.

Argenomics pioneers new test (Mitocount) to help select embryos which are more likely to result in viable pregnancies through In Vitro Fertilization (IVF).

One of the major reasons for the recurring pregnancy losses and IVF failures is a disorder occurring in the endometrium which mainly concerns abnormal gene expressions. Now using the procedure Endometrial Receptor Gene Assay (ERGA), it is possible to...

This is the prenatal genetic testing of foetal chromosomal aneuploidies from Mother’s Blood. We have the credit of being the first centre in the Indian subcontinent to develop in-house Non-Invasive Prenatal Testing (NIPT) which is 99.9% sensiti...

Pre-Implantation
Genetic Diagnosis (PGD)

PGD for Chromosomal Translocations: Preimplantation Genetic Diagnosis (PGD) – done on embryos created after IVF wherein the genetic diagnosis...

Pre-Implantation Genetic Screening (PGS)

24 chromosome PGS Pre-Implantation Genetic Screening (PGS) involves a process of screening of embryos in the course of In Vitro Fertilization (IVF). ...

  • cytogenetics

    Cytogenetics refers to the study of chromosome content in a cell. Argenomics has a fully equipped Cytogenetics lab with automated Karyotyping and FISH software. A complete Karyotype including structural chromosomal abnormalities and micro-deletions can be obtained using this facility. FISH is only performed on selected chromosomes. Cytogenetic studies can be done on a variety of samples like Peripheral blood, Amniotic fluid, CVS, and products of conception.

  • Hereditary Disease

    Targeted Mutation Screening  is a diagnostic tool completed through blood test that identifies the mutated gene or genes causing a genetic disease in your family. The identification of a gene mutations allows for further steps to be taken to prevent the passing on of the condition to future generations and may aid in the improvement of treatment of an affected individual. In most cases, after identifying the cause of genetic disease the couples can go with a Pre-Implantation Genetic Diagnosis (PGD) for Single Gene Disorders, a genetic test...

  • REPRODUCTIVE GENETICS

    Preconception genetic testing Pre-Implantation Genetic Screening (PGS) involves a process of screening of embryos in the course of In Vitro Fertilization (IVF). This helps to identify abnormalities in the chromosomes occurring due to aneuploidy. The main reason for recurrent IVF failures and in turn pregnancy losses is the higher risk of chromosomal errors that happ...