Vanishing Twin Syndrome

Vanishing Twin Syndrome is a condition that occurs in certain twin pregnancies.

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What is Vanishing Twin Syndrome?

Vanishing Twin Syndrome occurs when one twin in a multiple pregnancy disappears during gestation, often in the first trimester. This happens because one of the foetuses stops developing and is absorbed by the mother’s body or the surviving twin. Many women might not even realise they were carrying twins, as the only signs can be mild symptoms like slight cramping or bleeding. Early ultrasound scans may initially show two gestational sacs, but later only one is visible.

The exact cause of Vanishing Twin Syndrome isn’t always known, but it often involves chromosomal abnormalities in the undeveloped twin. The remaining twin usually continues to grow normally, and the pregnancy proceeds without further complications.

Vanishing Twin Syndrome statistics

15% to 36% Vanishing twin syndrome is estimated to occur in around 15% to 36% of twin pregnancies.
30% to 50% Rates are higher in higher-order multiple pregnancies of three or more gestational sacs, where it is reported in approximately 30% to 50% of cases.
20% to 30% It is thought to affect around 20% to 30% of pregnancies conceived through assisted reproductive technology such as IVF.
First trimester The loss of one twin usually happens in the first trimester, often before a woman is aware she is carrying more than one baby.
Around 60% Around 60% of vanishing twins are thought to carry a chromosomal abnormality. Because of this, residual DNA from a twin that has been lost can occasionally lead to a false-positive NIPT result.
Up to 15 weeks Cell-free DNA from a twin that has been lost can persist in the mother's blood for at least 7 to 8 weeks, and in some cases up to about 15 weeks, after the loss. Because this residual DNA can affect the reliability of NIPT, results are interpreted with care and testing may need to be repeated.
Vanishing Twins at 7 weeks
Twin Pregnancy Visualised in 3D Ultrasound Scan

Vanishing Twin Syndrome Facts and Statistics

Prevalence

Vanishing Twin Syndrome occurs in some twin or multiple pregnancies detected in the first trimester.

Early Occurrence

The phenomenon typically happens within the first 12 weeks of gestation, often before the mother is aware she’s carrying multiples.

Detection through Ultrasound

Advances in ultrasound technology have increased diagnosis rates. Early scans can now reveal multiple gestational sacs.

Chromosomal Abnormalities

The vanishing twin often has chromosomal abnormalities, which lead to its cessation of development and absorption.

Maternal Age Factor

Women over the age of 30 have a higher likelihood of experiencing Vanishing Twin Syndrome compared to younger women.

Impact on Remaining Foetus

The surviving twin usually continues to develop normally, and the pregnancy proceeds without significant complications.

Assisted Reproductive Technologies

The use of treatments like in vitro fertilisation (IVF) has led to an increase in multiple pregnancies and, consequently, instances of Vanishing Twin Syndrome.

Vanishing Twin and NIPT – challenges and recent developments

Performing Non-Invasive Prenatal Testing (NIPT) in pregnancies affected by Vanishing Twin Syndrome can be challenging due to the presence of residual DNA from the demised twin. NIPT analyses cell-free fetal DNA circulating in the mother’s bloodstream to screen for chromosomal abnormalities. In cases where one twin has ceased to develop, its genetic material may still linger in the maternal blood.

This residual DNA can interfere with the test results, potentially leading to false positives or inconclusive findings, as the test may detect chromosomal anomalies from the non-viable twin rather than the healthy one.

3d visualisation of a baby at 10 weeks
3d visualisation of a baby at 10 weeks

Vanishing twin and NIPT: recent developments

Recent technological advances have begun to address these challenges. They improve the accuracy of NIPT testing. Enhanced bioinformatics algorithms and more sophisticated DNA sequencing techniques allow for better differentiation between the DNA of the surviving twin and that of the vanished one. These innovations reduce the likelihood of false-positive results, providing more accurate and reliable screenings for expectant mothers experiencing Vanishing Twin Syndrome.

At LPC, we offer 2 tests that can work with Vanishing Twins; PrenatalSafe NIPT and PrenatalSafe Complete Plus NIPT. You have to wait at least 5 weeks post the diagnosis of the vanishing twin on ultrasound to do the NIPT.

Some of the questions our specialists can help with…

What is Vanishing Twin Syndrome?

Vanishing Twin Syndrome occurs when one twin in a multiple pregnancy disappears during gestation, often in the first trimester. This happens because one of the foetuses stops developing and is absorbed by the mother’s body or the surviving twin. Many women may not even realise they were carrying twins, as the only signs can be mild symptoms such as slight cramping or bleeding. An early ultrasound scan may initially show two gestational sacs, but later only one is visible.

Read more in our Blog

What Causes Vanishing Twin Syndrome?

The exact cause of Vanishing Twin Syndrome isn’t always known, but it often involves chromosomal abnormalities in the undeveloped twin. These abnormalities can lead the affected twin to stop developing and be gradually absorbed. In most cases the remaining twin continues to grow normally and the pregnancy proceeds without further complications.

How Common is Vanishing Twin Syndrome?

Vanishing Twin Syndrome occurs in some twin or multiple pregnancies detected in the first trimester. It typically happens within the first 12 weeks of gestation, often before the mother is aware she is carrying multiples. Advances in ultrasound technology have increased diagnosis rates, as early scans can now reveal multiple gestational sacs. The wider use of assisted reproductive technologies such as in vitro fertilisation (IVF) has also increased the number of multiple pregnancies and, consequently, instances of the condition.

What are the Symptoms of Vanishing Twin Syndrome?

Many women experience no noticeable symptoms at all, which is why the condition is often only identified on an ultrasound scan. Where symptoms do occur, they can be mild — for example slight cramping or bleeding. Because these signs are non-specific and common in early pregnancy, they do not on their own confirm a vanishing twin.

If you have concerns about your pregnancy or baby's wellbeing, contact your midwife, GP, or maternity unit promptly.

How is Vanishing Twin Syndrome Diagnosed?

Vanishing Twin Syndrome is usually identified through ultrasound. An early scan may initially show two gestational sacs, while a later scan shows only one, indicating that one twin has stopped developing and is being absorbed. Advances in ultrasound technology have improved detection, as early scans can now reveal multiple gestational sacs more clearly.

Can Vanishing Twin Syndrome Affect the Surviving Twin?

In most cases the surviving twin continues to develop normally and the pregnancy proceeds without significant complications. The remaining twin usually grows as expected once the other twin has been absorbed. Your specialist can monitor the pregnancy with ultrasound and discuss what to expect in your individual circumstances.

Is There Any Treatment for Vanishing Twin Syndrome?

Vanishing Twin Syndrome is generally not a condition that is treated, as it reflects a natural process in early pregnancy where one twin stops developing and is absorbed. In most cases the surviving twin continues to grow normally and the pregnancy proceeds without significant complications. Care usually focuses on monitoring the ongoing pregnancy with ultrasound rather than any specific intervention. Please discuss your individual circumstances with our specialists, who can advise on appropriate monitoring for you.

This information is intended for general educational purposes only and does not constitute medical advice. Please consult a qualified healthcare professional for guidance specific to your individual circumstances.

Does Vanishing Twin Syndrome Increase Pregnancy Risks?

In most cases, once one twin has been absorbed the surviving twin continues to develop normally and the pregnancy proceeds without significant complications. Because individual circumstances vary, any specific concerns about your pregnancy are best discussed with our specialists, who can review your scans and history. This information is intended for general educational purposes only and does not constitute medical advice.

If you have concerns about your pregnancy or baby's wellbeing, contact your midwife, GP, or maternity unit promptly.

How Does Vanishing Twin Syndrome Impact the Mother Emotionally?

Learning about a vanishing twin can be an emotional experience, and it is understandable to have a range of feelings even when the surviving twin is developing normally. Everyone responds differently, and there is no right or wrong way to feel. Our specialists are happy to talk through what the diagnosis means for you, and your midwife or GP can also point you towards further support if you would find it helpful.

This information is intended for general educational purposes only and does not constitute medical advice. Please consult a qualified healthcare professional for guidance specific to your individual circumstances.

Can Vanishing Twin Syndrome Affect NIPT Results?

Yes. Non-Invasive Prenatal Testing (NIPT) analyses cell-free fetal DNA circulating in the mother’s bloodstream, and in a vanishing twin pregnancy residual DNA from the demised twin may still be present. This residual DNA can interfere with results, potentially leading to false positives or inconclusive findings, as the test may detect chromosomal anomalies from the non-viable twin rather than the healthy one. Recent advances in bioinformatics and DNA sequencing have improved accuracy by better distinguishing between the DNA of the surviving and vanished twins.

At LPC we offer two tests that can work with vanishing twins: PrenatalSafe NIPT and PrenatalSafe Complete Plus NIPT. You need to wait at least 5 weeks after the vanishing twin is diagnosed on ultrasound before having the NIPT.

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Sources & clinical references

The figures and clinical statements on this page are drawn from the sources below. Guidance evolves — always discuss your individual circumstances with a clinician.

  1. StatPearls Publishing (NCBI Bookshelf)Vanishing Twin Syndrome2025
  2. Clinical Case Reports (Wiley)Discordant NIPT result in a viable trisomy-21 pregnancy due to prolonged contribution to cfDNA by a demised trisomy-14 cotwin2018
  3. Journal of Clinical Medicine (MDPI)Fetal Aneuploidy Detection by Cell-Free DNA Sequencing for Multiple Pregnancies and Quality Issues with Vanishing Twins2014