PGS (Preimplantation genetic screening)

PGS is a genetic test performed on embryos created through IVF. It examines the number of chromosomes in each embryo to detect abnormalities that may cause implantation failure, miscarriage, or genetic disorders like Down syndrome. Selecting chromosomally normal embryos increases the likelihood of a healthy pregnancy.

Who Should Consider PGS?

PGS is recommended for couples who:

Have experienced recurrent pregnancy loss or failed IVF cycles

Are of advanced maternal age (35 years or older)

Have a history of chromosomal abnormalities

Want to improve embryo selection during IVF

Have a family history of genetic conditions

The PGS Process

1. Ovarian Stimulation & Egg Retrieval:

IVF begins with ovarian stimulation, followed by egg retrieval and fertilization in the lab.

2. Embryo Development

Embryos are cultured for several days until they reach the blastocyst stage.

3. Embryo Biopsy

A few cells are carefully taken from each embryo for genetic analysis.

4. Chromosomal Analysis

The cells are tested to identify any chromosomal abnormalities.

5. Embryo Selection & Transfer

Only chromosomally normal embryos are selected for implantation, enhancing the chances of a successful pregnancy.

Why Choose Manasi Clinic for PGS?

Expertise in ART: Specialized in advanced fertility treatments with high success rates

State-of-the-Art Facilities: Cutting-edge genetic screening and IVF technologies

Personalized Care: Customized treatment plans to meet each couple’s unique needs

Comprehensive Support: Guidance from pre-conception counseling through successful pregnancy