Skip to content
EN-MY
Book now
Book now

Sunfert IVF With PGT-M Package

IVF treatment with PGT-M screening helps reduce the risk of passing inherited genetic disorders to your baby and breaks the cycle of genetic disorders for future generations
Helpful tools

What is Sunfert IVF With PGT-M?

IVF with PGT-M Package combines personalised fertility treatment with advanced reproductive technologies such as Pre-Implantation Genetic Testing for Monogenic Disorder (PGT-M) and Time-Lapse Embryo Imaging, allowing our clinical team to identify embryos that are free from specific inherited genetic disorders before implantation.

This innovative approach provides you and your spouse with a chance to reduce the risk of passing on monogenic disorders, supporting a healthier pregnancy and increasing confidence in your IVF journey.

Who Should Consider Sunfert IVF With PGT-M?

Couples who:

  • are carriers of a known genetic disorder
  • have a family history of inherited diseases
  • have previously had a child affected by a genetic condition
  • want to minimise the risk of passing an inherited genetic disorder to their child

Our fertility specialists will review your medical history, fertility health and genetic carrier screening results to determine if IVF with PGT-M is the best option for your family planning.

How Sunfert IVF With PGT-M Can Help?

Personalised Fertility Treatment

  • Our specialists carefully evaluate your reproductive health, medical history, and genetic risk factors to create a dedicated fertility treatment plan. This personalised approach optimises your chances of a successful pregnancy while addressing your unique parenthood goals.

 

Time-Lapse Embryo Imaging

  • At Sunfert, we use industry-leading Time-Lapse Embryo Imaging technology, which is known as the EmbryoScope™, to continuously monitor your embryos’ development within a stable incubator environment, minimising disturbance and supporting optimal growth conditions.
  • High-resolution images captured at regular intervals provide detailed insights into each embryo’s development, allowing our embryologists to assess both appearance and growth patterns for more accurate selection.
  • Combined with AI-supported evaluation tools, this technology enhances precision, reduces subjectivity, and supports more informed decisions in selecting embryos with higher implantation potential.

 

PGT-M Screening

  • Our genetic scientists perform PGT-M using advanced Karyomapping technology to identify embryos affected by specific single gene conditions before transfer. This ensures that only embryos free from targeted inherited disorders such as thalassaemia, cystic fibrosis, or spinal muscular atrophy are selected for implantation.
  • By selecting embryos without known genetic disorders, the risk of miscarriage can be reduced, the chances of a healthy pregnancy are improved, and couples undergoing IVF are provided with greater reassurance and peace of mind throughout their fertility journey.

What Is Included in the Sunfert IVF With PGT-M Package?

1. Pre-PGT-M Work-Up

2. Doctor’s fees

3. All standard medications including:

  • Hormone injections until day of embryo transfer
  • Endometrial preparations (luteal support) until day of pregnancy test

4. Sedation by anaesthetist

5. Operating theatre charges

6. IVF lab procedures

7. Time-Lapse Embryo Imaging for up to 12 - 16 embryos using EmbryoScope™

8. PGT-M chargeable per blastocyst

  • PGT-M is a personalised genetic test where each embryo is assessed individually. By charging per blastocyst, patients only pay for what is needed, with the flexibility to decide when and how many embryos to test. Thereby, giving you greater control, fairness and cost clarity.

9. Frozen Embryo Transfer (FET)

Why Choose Sunfert?

Prominent and Experienced Fertility Specialists

  • Our fertility specialist has extensive expertise in assisted reproductive treatments.

Well-trained Embryologists and Genetic Scientists

  • Advanced lab procedures ensure the highest standards for your embryos.

World-Class Fertility Technology and Laboratory Standards

  • Integrate advanced fertility technologies into the treatment journey to maximise your chances of success.

Patient-First Experience

  • Personalised care and 24/7 support throughout your fertility journey.

Proven Success Rate

  • Our track record demonstrates results that inspire confidence.

Range of Payment Options

  • We provide personalised financial counselling, offering a variety of payment options and support designed just for you.

Take the Next Step with Our Fertility Specialists

If you are facing fertility challenges, start with a consultation with our specialists. We will guide you through your fertility journey with expertise and compassionate care. 

Make an appointment with our Fertility Specialist today and take the next step toward your parenthood goals.

What is Pre-implantation Genetic Testing for Monogenic Disorder (PGT-M) in IVF?

Pre-implantation Genetic Testing for Monogenic Disorder (PGT-M) is an advanced genetic test performed during IVF to detect specific inherited genetic disorders caused by mutations in a single gene.

It allows our fertility specialists to identify embryos that are unaffected before transfer, helping reduce the risk of passing genetic diseases to the baby.

What is Sunfert IVF with PGT-M Package?

IVF with PGT-M is a fertility treatment that combines In-vitro Fertilisation (IVF) with Pre-Implantation Genetic Testing for Monogenic Disorders (PGT-M).

It allows embryos to be tested for specific inherited genetic conditions before transfer.

This helps select embryos free from targeted disorders, supporting healthier pregnancy outcomes and reducing the risk of passing on genetic diseases.

Who should consider Sunfert IVF with PGT-M Package?

IVF with PGT-M is recommended for couples who:

  • are carriers of known genetic disorders
  • have a family history of inherited diseases
  • have previously had a child affected by a genetic condition
  • wish to reduce the risk of passing on monogenic disorders.

Our fertility specialist will assess medical and genetic history to determine suitability.

What genetic disorders can PGT-M detect?

PGT-M can screen for many inherited single-gene disorders, including: 

  • Thalassaemia (common in Malaysia and Asia)
  • Cystic Fibrosis
  • Huntington’s disease
  • Spinal Muscular Atrophy (SMA)
  • Certain metabolic and neurological genetic conditions

Can PGT-M help reduce miscarriage risk?

Yes, in some cases. By selecting embryos that are free from specific genetic disorders, PGT-M may lower the risk of miscarriage associated with inherited conditions, supporting a healthier pregnancy outcome.

Does PGT-M improve IVF success rates?

PGT-M does not directly increase implantation rates, but it improves the likelihood of transferring embryos that are free from specific genetic disorders.

This contributes to better pregnancy outcomes and reduces the risk of inherited disease.

Can PGT-M prevent genetic diseases completely?

PGT-M significantly reduces the risk of passing specific inherited genetic disorders by selecting unaffected embryos.

However, it does not guarantee a completely disease-free baby, as it targets only specific known gene mutations.

How long does the PGT-M process take?

The timeline varies depending on the complexity of the genetic condition. Typically: 

  • Genetic preparation and probe development may take several weeks
  • IVF cycle and embryo testing follow afterwards 

Your fertility specialist will provide a personalised timeline based on your case.

What is karyomapping and why is it used in PGT-M?

Karyomapping is a sophisticated genetic testing technique that tracks the inheritance of DNA segments from both parents.

It helps identify whether an embryo has inherited a specific gene mutation.

This method improves the accuracy of detecting monogenic disorders and supports safer embryo selection.

When should I speak to a fertility specialist about PGT-M?

You should consult a fertility specialist if you:

  • know you or your partner carries a genetic condition
  • have a family history of inherited disorders
  • have experienced previous genetic-related pregnancy loss
  • wish to explore safer IVF options

At Sunfert, our fertility specialists can help determine whether PGT-M is suitable for your situation. Transparency and honesty are core to our values.

We ensure that any additional procedures are recommended only when there is clear clinical benefit, so patients do not undergo or incur costs for treatments that are not necessary for their fertility journey.

Is PGT-M necessary for all IVF patients?

No. PGT-M is not required for every IVF patient. It is mainly advised for couples with a known risk of passing on specific genetic disorders. Our fertility specialist will recommend PGT-M based on medical history, genetic screening results, and individual circumstances.

If you are unsure whether you or your partner are carriers of certain genetic conditions, you may consider undergoing an Expanded Carrier Screening (ECS) blood test for further assessment.

Is embryo biopsy safe during PGT-M?

Embryo biopsy is a highly specialised procedure performed at the blastocyst stage.

At Sunfert, this procedure are conducted by highly experienced and well-trained embryologists and genetic scientists using established protocols, hence we can assure our patients it is safe and would not affect the embryo development.

Ready to start your fertility journey?

Book now

The Biological Clock

This tool indicates:

  • Natural conception per month if you have no fertility issues
  • IVF success rate at the same age
  • When to seek help after months of unsuccessful attempts

If you are concerned at any stage – we recommend booking a doctor appointment or a free nurse consultation. The sooner you make a plan the better your chances in the long term.

When to seek advice early

If you have polycystic ovaries, endometriosis, or have been through a cancer diagnosis; we recommend you get in touch quickly so we can talk you through all your options and give you the greatest possible chance of success.

If you’re a single woman considering motherhood in the future; it’s best to approach us early and consider egg freezing as this can be an option for you while you have a higher ovarian reserve and healthier eggs.

Set your age and the months you’ve been trying to conceive
26
2
Your chance of having a baby per month for fertile couples
Your chance of having a baby per IVF cycle (if experiencing infertility)

Body Mass Index calculator

Being overweight or underweight can reduce fertility, so it is important to keep your body weight within the normal healthy range.

Body Mass Index (BMI) is an indication of your body weight and can be calculated by dividing weight by height. You should aim for a BMI of between 20 and 25, as this will optimise your chances of conception.

Woman’s BMI below 19

Even in these modern times, nature knows best. If a woman's BMI falls below 19, the body senses famine and ovulation is switched off to prevent the risk of having a baby with malnutrition. Excessive exercise can reduce body fat and increase muscle mass to a point where periods cease for the same reason. Risk of miscarriage is also increased in women with a low BMI.

Being underweight

If a woman's BMI falls below 19, the body senses famine and ovulation is switched off to prevent the risk of having a baby with malnutrition. Excessive exercise can reduce body fat and increase muscle mass to a point where periods cease for the same reason. Risk of miscarriage is also increased in women with a low BMI.

BMI’s greater than 30

This can reduce fertility by 50%. Pregnancy for women with a 30+ BMI is often associated with problems such as maternal diabetes, high blood pressure, big babies and increased risk of caesarean section.

Add your height and weight to calculate your BMI
+603 7622 8688