By Healthtrip Blog Published on - 30 September - 2023

Choosing the Right Path: PGT-A and PGT-M in Family Planning


In the realm of assisted reproductive technology, In Vitro Fertilization (IVF) has been a groundbreaking advancement, offering hope to couples struggling with infertility. However, as science continues to progress, so do the techniques and options available within IVF. One of the most significant developments in recent years has been the introduction of Preimplantation Genetic Testing (PGT). Within PGT, there are two primary methods: PGT-A (Aneuploidy screening) and PGT-M (Monogenic disorder testing). In this blog, we will explore these two techniques, their differences, and their implications for prospective parents.

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1. PGT-A: Ensuring Chromosomal Normalcy

1.1 What is PGT-A?

PGT-A, or Preimplantation Genetic Testing for Aneuploidy, is a technique used to screen embryos for chromosomal abnormalities. Aneuploidy refers to an abnormal number of chromosomes in an embryo, which can lead to miscarriages, implantation failures, or genetic disorders in the offspring. PGT-A aims to identify and select embryos with the correct number of chromosomes, increasing the chances of a successful pregnancy.

1.2. How Does PGT-A Work?

  • Embryo Biopsy: After fertilization in the IVF lab, embryos develop for about five days. At this stage, a few cells are carefully extracted from each embryo, without causing harm.
  • Genetic Analysis: The extracted cells are then analyzed to determine the chromosomal makeup of each embryo. This process is typically performed using techniques like Next-Generation Sequencing (NGS) or Comparative Genomic Hybridization (CGH).
  • Selection: Based on the genetic analysis, embryos with the correct number of chromosomes are selected for implantation.

1.3. Pros of PGT-A

  • Increased Pregnancy Success: By selecting chromosomally normal embryos, the likelihood of successful implantation and a healthy pregnancy is significantly improved.
  • Reduced Risk of Miscarriage: Aneuploid embryos are a leading cause of miscarriages. PGT-A helps reduce this risk.
  • Fewer Selective Reductions: Reducing the number of embryos implanted can be an option in cases of multiple pregnancies. PGT-A minimizes the need for this.

2. PGT-M: Targeting Genetic Disorders

2.1. What is PGT-M?

Preimplantation Genetic Testing for Monogenic disorders (PGT-M) is a technique designed to identify specific genetic mutations or disorders within embryos. This is particularly relevant when one or both prospective parents carry a known genetic disease or have a family history of such conditions.

2.2. How Does PGT-M Work?

  • Genetic Testing: Before IVF, both prospective parents undergo genetic testing to identify any known genetic mutations. If a specific mutation is identified, PGT-M can be tailored to detect that particular mutation in embryos.
  • Embryo Biopsy: Similar to PGT-A, embryos are biopsied to extract a few cells.
  • Mutation Screening: The extracted cells are analyzed to determine whether the embryos carry the targeted genetic mutation.
  • Selection: Embryos without the mutation are chosen for implantation.

2.3. Pros of PGT-M

  • Preventing Genetic Disorders: PGT-M enables couples at risk of passing on a genetic disease to have healthy children without the disease.
  • Ethical Consideration: It avoids the moral dilemma of whether to terminate a pregnancy if a genetic disorder is identified after conception.
  • Peace of Mind: Parents can have confidence that their child will not inherit a known genetic disorder.

3. Choosing Between PGT-A and PGT-M

The decision between PGT-A and PGT-M depends on the specific needs and circumstances of each couple.

  • PGT-A is for couples seeking to improve overall pregnancy success rates by selecting embryos with the correct chromosomal count.
  • PGT-M is for couples at risk of passing on a known genetic disorder to their offspring.

The choice often involves medical, ethical, and emotional considerations. While PGT-A focuses on general chromosomal health, PGT-M addresses a specific genetic concern within a family's medical history.

4. The Future of Family Planning

The future of family planning through IVF is exciting and filled with possibilities, thanks to PGT-A and PGT-M. However, it's essential to consider some key points:

4.1. Ethical and Societal Implications

The ability to select embryos based on genetic traits raises ethical questions about "designer babies" and the potential for genetic discrimination. Society must grapple with these issues while advancing the field responsibly.

4.2. Accessibility and Costs

Currently, PGT-A and PGT-M can be expensive, making them inaccessible to some couples. The future will hopefully bring advancements that make these technologies more affordable and widely available.

4.3. Ongoing Research

Research into genetic screening techniques and the understanding of various genetic disorders is continually evolving. The future holds promise for even more precise and reliable testing methods.


The future of family planning is being reshaped by innovative technologies like PGT-A and PGT-M. These techniques offer hope to couples facing fertility challenges and genetic disorders, but they also bring ethical and societal considerations to the forefront. As science and technology advance, it is crucial that we navigate these uncharted waters with wisdom and compassion, ensuring that the future of family planning remains a source of joy, hope, and healthy generations to come.

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In Vitro Fertilization (IVF) is a reproductive technology that involves fertilizing an egg with sperm outside the body in a laboratory. The resulting embryos are then implanted into the uterus.
Preimplantation Genetic Testing for Aneuploidy (PGT-A) is used in IVF to screen embryos for chromosomal abnormalities. It helps select embryos with the correct chromosomal count, improving pregnancy success rates.
Preimplantation Genetic Testing for Monogenic Disorders (PGT-M) is used when couples have a known genetic disorder in their family. It helps prevent the transmission of specific genetic diseases to their children.
PGT-A increases the chances of a successful pregnancy, reduces the risk of miscarriage, and allows for the transfer of healthy embryos
PGT-M identifies embryos without the targeted genetic mutation, ensuring that only healthy embryos are implanted, preventing the inheritance of genetic disorders.
These technologies raise ethical questions about selecting certain traits in embryos, the potential for "designer babies," and genetic discrimination. Ethical guidelines are being developed to address these concerns.
Currently, these technologies can be expensive and may not be accessible to all couples. Efforts are ongoing to make them more widely available and affordable.
Success rates can vary depending on several factors, including the age and health of the parents and the specific genetic conditions involved. Consulting with a fertility specialist is recommended for personalized information.
Yes, there are alternatives, such as traditional IVF without genetic testing, adoption, and using donor eggs or sperm. The choice depends on individual circumstances and preferences.
The future promises advancements in genetic testing technology, improved affordability, and a deeper understanding of genetic disorders, providing more options for couples seeking to build healthy families.
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