NIPT vs NICC: What Is the Difference and Which Test Is Right for You?
Finding out you are pregnant is one of the most emotionally charged moments in a woman’s life. Within days, the questions start coming, and they do not stop. Is my baby healthy? Should I be worried? What tests do I need to do and when?
If you have been researching prenatal screening, you have probably come across two terms that look almost identical: NIPT and NICC. It is completely understandable to feel confused. Many mothers who visit us at Klinik Caring in Johor Bahru ask us exactly this question, sometimes after spending hours searching online and feeling more confused than when they started.
So let us clear this up once and for all.
This article explains what NIPT and NICC are, how they are different, what the Basic screening involves compared to the more advanced DNA-based options, and how to decide which is right for your pregnancy. We have written this in plain language, because you deserve a straight answer, not a lecture.
At Klinik Caring, located in Impian Emas, Skudai, Johor Bahru, our female doctor sees pregnant mothers from across Johor Bahru, Skudai, Nusajaya, and Singapore every week. This article reflects the same explanation she gives in the consultation room.
Every human being has 46 chromosomes, arranged in 23 pairs. These chromosomes carry the genetic instructions that shape your baby’s development from the very beginning. Occasionally, a baby may be born with an extra or missing chromosome. This is called a chromosomal abnormality, and depending on which chromosome is affected, it can have a significant impact on your baby’s physical health, development, and quality of life.
The most well-known chromosomal condition is Down Syndrome, also called Trisomy 21. This happens when a baby has three copies of chromosome 21 instead of the usual two. Other conditions include Edwards Syndrome (Trisomy 18) and Patau Syndrome (Trisomy 13). There are also conditions involving the sex chromosomes, rare microdeletion syndromes, and inherited single-gene disorders.
Here is something important to understand: chromosomal conditions can happen in any pregnancy. While the risk does increase with the mother’s age, younger mothers are not exempt. This is why prenatal chromosomal screening is offered to all pregnant mothers, regardless of age.
Prenatal chromosomal screening allows you to assess the risk of these conditions during pregnancy, safely and without any procedure that puts your baby at risk.
Here is how it works. During pregnancy, small fragments of your baby’s DNA enter your bloodstream. These are called cell-free fetal DNA (cfDNA). A simple blood draw from the mother is all that is needed. In the laboratory, scientists analyse these DNA fragments to screen for chromosomal abnormalities with a very high level of accuracy.
What makes NIPT stand out is its detection rate. For Down Syndrome (Trisomy 21), NIPT has a detection rate of over 99%. That is significantly higher than older screening methods.
Key points about NIPT:
NIPT requires only a simple blood draw from the mother. No risk to the baby.
This is the most important thing to understand: NICC is not a single test. It is a programme that covers two different types of screening technology under one name:
This distinction matters, and understanding it will help you make the right choice for your pregnancy.
1. Nuchal Translucency (NT) Ultrasound Scan
This is a specialised ultrasound scan done between 11 and 13 weeks of pregnancy. The doctor or sonographer measures the fluid-filled space at the back of your baby’s neck. This measurement is called the nuchal translucency. A measurement that is larger than normal can suggest a higher risk of chromosomal conditions such as Down Syndrome.
This scan also allows the doctor to check your baby’s heartbeat, position, and early development, which makes it a valuable appointment beyond just the chromosomal screening aspect.
The Nuchal Translucency (NT) ultrasound is performed between 11 and 13 weeks of pregnancy.
2. Free Beta-hCG (Free Beta Human Chorionic Gonadotropin)
This is a hormone produced by the placenta, measured through a blood test. Abnormal levels of Free Beta-hCG in early pregnancy can be associated with an increased risk of certain chromosomal conditions.
3. PAPP-A (Pregnancy-Associated Plasma Protein A)
This is another placental hormone, measured through the same blood test. Low levels of PAPP-A in the first trimester have been associated with a higher risk of chromosomal abnormalities.
By combining the NT measurement, the two blood hormone levels, and the mother’s age, the Basic NICC calculates a risk score for Trisomy 21 (Down Syndrome), Trisomy 18 (Edwards Syndrome), and Trisomy 13 (Patau Syndrome).
A result might read something like “1 in 1,500 risk for Down Syndrome,” which would be considered low risk, or “1 in 25 risk for Down Syndrome,” which would be considered high risk and would prompt a discussion about further testing.
Detection rate: Approximately 85 to 90% for Down Syndrome.
Timing: Must be done between 11 and 13 weeks and 6 days of pregnancy. The NT ultrasound is only reliable within this specific window.
What the result means: The Basic NICC gives a risk estimate, not a yes or no answer. A low-risk result is genuinely reassuring for the majority of mothers. A high-risk result does not mean your baby definitely has a chromosomal condition. It means further investigation is recommended, and your doctor will guide you on what that looks like.
Rather than calculating risk from indirect markers like hormone levels and ultrasound measurements, NIPT-based packages examine your baby’s actual genetic material. This is why the accuracy is so much higher.
Detection rate: Over 99% for Down Syndrome (Trisomy 21).
Timing: Can be done from 10 weeks of pregnancy onwards.
What they screen for: Beyond the three main trisomy conditions, NIPT-based NICC packages can screen for sex chromosome abnormalities, microdeletion syndromes, inherited single-gene disorders carried by the mother, and de novo genetic mutations in the baby, depending on the package level chosen.
Gender identification is also available with all NIPT-based packages from 10 weeks onwards.
One thing worth noting: NIPT-based tests do not include an ultrasound scan as part of the test itself. If you would like an ultrasound alongside your NIPT, this can be arranged separately with your doctor.
(To learn more about what the different NICC package tiers cover, please check out our packages)
Here is a simple way to think through it.
The Basic NICC may be appropriate if you are between 11 and 13 weeks of pregnancy, you want the NT ultrasound included as part of your screening, and you understand that the result will be a risk estimate rather than a direct DNA finding. It is a well-established, clinically recognised approach that has guided prenatal care for many years.
NIPT-based NICC packages may be more suitable if you want the highest possible accuracy from a DNA-based result, you are at least 10 weeks pregnant, you want to know your baby’s gender, you are 35 years of age or older, you have had a previous pregnancy affected by chromosomal conditions, or you have a family history of genetic disorders.
Something worth considering: If your Basic NICC comes back as high risk, your doctor will likely recommend either a NIPT-based test or an invasive diagnostic test for further clarification. Some mothers, particularly those who find waiting difficult or who have specific risk factors, choose to start with a NIPT-based package directly to avoid the uncertainty of an intermediate result.
There is no wrong choice here. What matters is that you make an informed decision with full understanding of what each approach involves. That is exactly what our doctor at Klinik Caring is here to help you with.
Invasive tests are diagnostic, not screening. They provide a definitive answer rather than a risk estimate. However, they involve inserting a needle into the womb to collect a sample of amniotic fluid or placental tissue. This carries a small but real risk of miscarriage, estimated at approximately 0.5 to 1%.
For this reason, invasive testing is generally only recommended in specific situations: when a screening result has returned high risk, when there is a known family history of a chromosomal condition, or when other clinical factors suggest elevated risk.
Think of NICC screening as your first step. For the vast majority of mothers, results will be reassuring and invasive testing will never be needed. But when a screening result raises concern, knowing that next steps exist and that your doctor will guide you through them calmly is something we hope brings you comfort.
Female doctor: Our clinic is led by a female physician. For many mothers, especially when it comes to pregnancy and sensitive women’s health matters, having a female doctor makes a real difference to how comfortable and safe they feel. This is one of the most common reasons patients tell us they chose Klinik Caring.
We explain, not just report: Receiving a test result without proper explanation can be frightening, especially if the numbers mean nothing to you. At Klinik Caring, our doctor goes through your results with you in plain language, answers every question you have, and makes sure you leave the consultation feeling informed rather than anxious.
Full range of options under one roof: From the Basic NICC to the most comprehensive NIPT-based packages, everything is available at our clinic. You do not need to visit multiple specialists or hospitals to access different levels of screening.
Convenient location for Singapore patients: Our clinic is located in Impian Emas, Skudai, Johor Bahru, which is easily accessible from the Johor-Singapore Causeway. Many Singapore patients find this a practical and comfortable option for their prenatal care needs.
A clinic built on education: Our philosophy at Klinik Caring is “Medicate some days. Educate always.” We believe that an informed mother is an empowered mother. Every consultation is an opportunity to help you understand your health and your baby’s health more deeply.
A: Not exactly. NIPT is an internationally recognised term for cell-free fetal DNA prenatal testing. NICC is Klinik Caring’s prenatal screening programme, which includes both Basic (combined first trimester screening) and higher-tier packages that use NIPT technology. So the Standard NICC and above are NIPT-based, but the Basic NICC is not.
Q: Can NIPT or NICC give a definitive diagnosis of Down Syndrome?
A: No. Both are screening tests, not diagnostic tests. They provide a risk assessment, not a confirmed diagnosis. If results indicate high risk, your doctor will discuss further diagnostic options such as amniocentesis. That said, NIPT-based packages have a detection rate of over 99% for Down Syndrome, making them highly reliable as a screening tool.
Q: I am 9 weeks pregnant. Can I do the test now?
A: For NIPT-based packages, the recommended starting point is 10 weeks. For the Basic NICC, the window is 11 to 13 weeks. If you are 9 weeks today, you may wish to wait just one more week before coming in. Contact us via WhatsApp and we will help you plan the best timing.
Q: I am 35 years old. Does that mean I must do NIPT?
A: There is no strict requirement. However, the risk of chromosomal conditions does increase with maternal age, and many mothers aged 35 and above choose NIPT-based packages for the higher accuracy and broader coverage it provides. Your doctor will help you assess what is appropriate for your individual situation.
Q: I am travelling from Singapore. Do I need to book in advance?
A: Yes, we strongly recommend booking in advance via WhatsApp at 013-943 3314. This ensures our doctor is ready for your consultation and all necessary arrangements for your test are prepared before you make the trip.
Q: What happens after I receive my results?
A: Our doctor will review your results with you in detail during your consultation. For low-risk results, you will receive clear reassurance and guidance for your ongoing pregnancy care. For high-risk results, our doctor will explain your options clearly and support you through the next steps in a calm and caring manner. You will never be left to figure it out alone.
For the Basic NICC, the NT ultrasound window closes at 13 weeks and 6 days. Once that window passes, this particular screening option is no longer available.
For NIPT-based NICC packages, testing can begin from 10 weeks. The earlier you test, the more time you have to receive results, process the information, and take any necessary next steps.
Our honest advice: as soon as your pregnancy is confirmed, make an appointment to discuss your prenatal screening options. Even if you are still in the very early weeks, a brief consultation can help you plan ahead with confidence.
If you are unsure which test is right for you, that is exactly what our doctor at Klinik Caring is here for.
At Klinik Caring in Impian Emas, Skudai, Johor Bahru, our female doctor will sit with you, listen to your concerns, explain your options clearly, and help you make a decision that feels right for you and your baby.
Whether you are from Johor Bahru, Skudai, Nusajaya, or travelling from Singapore, we welcome you.
WhatsApp us today to book your appointment:
📱 013-943 3314
📍 No. 16-01, Jalan Bukit Impian 18/5, Taman Impian Emas, 81300 Skudai, Johor
🌐 www.klinikcaring.com
This article is written for educational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Please consult a qualified doctor for personalised guidance regarding your pregnancy.
If you have been researching prenatal screening, you have probably come across two terms that look almost identical: NIPT and NICC. It is completely understandable to feel confused. Many mothers who visit us at Klinik Caring in Johor Bahru ask us exactly this question, sometimes after spending hours searching online and feeling more confused than when they started.
So let us clear this up once and for all.
This article explains what NIPT and NICC are, how they are different, what the Basic screening involves compared to the more advanced DNA-based options, and how to decide which is right for your pregnancy. We have written this in plain language, because you deserve a straight answer, not a lecture.
At Klinik Caring, located in Impian Emas, Skudai, Johor Bahru, our female doctor sees pregnant mothers from across Johor Bahru, Skudai, Nusajaya, and Singapore every week. This article reflects the same explanation she gives in the consultation room.
First, What Is Prenatal Chromosomal Screening?
Before comparing NIPT and NICC, it helps to understand what these tests are actually looking for.Every human being has 46 chromosomes, arranged in 23 pairs. These chromosomes carry the genetic instructions that shape your baby’s development from the very beginning. Occasionally, a baby may be born with an extra or missing chromosome. This is called a chromosomal abnormality, and depending on which chromosome is affected, it can have a significant impact on your baby’s physical health, development, and quality of life.
The most well-known chromosomal condition is Down Syndrome, also called Trisomy 21. This happens when a baby has three copies of chromosome 21 instead of the usual two. Other conditions include Edwards Syndrome (Trisomy 18) and Patau Syndrome (Trisomy 13). There are also conditions involving the sex chromosomes, rare microdeletion syndromes, and inherited single-gene disorders.
Here is something important to understand: chromosomal conditions can happen in any pregnancy. While the risk does increase with the mother’s age, younger mothers are not exempt. This is why prenatal chromosomal screening is offered to all pregnant mothers, regardless of age.
Prenatal chromosomal screening allows you to assess the risk of these conditions during pregnancy, safely and without any procedure that puts your baby at risk.
What Is NIPT?
NIPT stands for Non-Invasive Prenatal Testing. It is the internationally recognised term used in Singapore, the United Kingdom, Australia, the United States, and most parts of the world.Here is how it works. During pregnancy, small fragments of your baby’s DNA enter your bloodstream. These are called cell-free fetal DNA (cfDNA). A simple blood draw from the mother is all that is needed. In the laboratory, scientists analyse these DNA fragments to screen for chromosomal abnormalities with a very high level of accuracy.
What makes NIPT stand out is its detection rate. For Down Syndrome (Trisomy 21), NIPT has a detection rate of over 99%. That is significantly higher than older screening methods.
Key points about NIPT:
- Only a blood draw is required from the mother
- Can be done from as early as 10 weeks of pregnancy
- Detection rate of over 99% for Down Syndrome
- Screens for a wide range of chromosomal conditions
- Completely non-invasive, no risk of miscarriage from the test
- It is a screening test, not a definitive diagnosis
NIPT requires only a simple blood draw from the mother. No risk to the baby.
What Is NICC?
NICC stands for Non-Invasive Chromosomal Check. At Klinik Caring, NICC is the name we use for our complete prenatal chromosomal screening programme.This is the most important thing to understand: NICC is not a single test. It is a programme that covers two different types of screening technology under one name:
- Basic NICC uses combined first trimester screening technology, which is a well-established method that combines an ultrasound measurement with blood hormone markers.
- Standard NICC and above use NIPT technology, meaning direct cell-free fetal DNA analysis from the mother’s blood.
This distinction matters, and understanding it will help you make the right choice for your pregnancy.
The Key Difference: Basic NICC vs NIPT-Based Packages
This is the section that most mothers tell us they wished they had read sooner. Let us go through each one carefully.Basic NICC: Combined First Trimester Screening
The Basic NICC is what doctors call Combined First Trimester Screening. It does not analyse your baby’s DNA directly. Instead, it combines three pieces of information to calculate a risk score for chromosomal conditions.1. Nuchal Translucency (NT) Ultrasound Scan
This is a specialised ultrasound scan done between 11 and 13 weeks of pregnancy. The doctor or sonographer measures the fluid-filled space at the back of your baby’s neck. This measurement is called the nuchal translucency. A measurement that is larger than normal can suggest a higher risk of chromosomal conditions such as Down Syndrome.
This scan also allows the doctor to check your baby’s heartbeat, position, and early development, which makes it a valuable appointment beyond just the chromosomal screening aspect.
The Nuchal Translucency (NT) ultrasound is performed between 11 and 13 weeks of pregnancy.
2. Free Beta-hCG (Free Beta Human Chorionic Gonadotropin)
This is a hormone produced by the placenta, measured through a blood test. Abnormal levels of Free Beta-hCG in early pregnancy can be associated with an increased risk of certain chromosomal conditions.
3. PAPP-A (Pregnancy-Associated Plasma Protein A)
This is another placental hormone, measured through the same blood test. Low levels of PAPP-A in the first trimester have been associated with a higher risk of chromosomal abnormalities.
By combining the NT measurement, the two blood hormone levels, and the mother’s age, the Basic NICC calculates a risk score for Trisomy 21 (Down Syndrome), Trisomy 18 (Edwards Syndrome), and Trisomy 13 (Patau Syndrome).
A result might read something like “1 in 1,500 risk for Down Syndrome,” which would be considered low risk, or “1 in 25 risk for Down Syndrome,” which would be considered high risk and would prompt a discussion about further testing.
Detection rate: Approximately 85 to 90% for Down Syndrome.
Timing: Must be done between 11 and 13 weeks and 6 days of pregnancy. The NT ultrasound is only reliable within this specific window.
What the result means: The Basic NICC gives a risk estimate, not a yes or no answer. A low-risk result is genuinely reassuring for the majority of mothers. A high-risk result does not mean your baby definitely has a chromosomal condition. It means further investigation is recommended, and your doctor will guide you on what that looks like.
Standard NICC and Above: NIPT Technology
From the Standard NICC package onwards, the technology is fundamentally different. These packages use NIPT technology, directly analysing cell-free fetal DNA from the mother’s blood.Rather than calculating risk from indirect markers like hormone levels and ultrasound measurements, NIPT-based packages examine your baby’s actual genetic material. This is why the accuracy is so much higher.
Detection rate: Over 99% for Down Syndrome (Trisomy 21).
Timing: Can be done from 10 weeks of pregnancy onwards.
What they screen for: Beyond the three main trisomy conditions, NIPT-based NICC packages can screen for sex chromosome abnormalities, microdeletion syndromes, inherited single-gene disorders carried by the mother, and de novo genetic mutations in the baby, depending on the package level chosen.
Gender identification is also available with all NIPT-based packages from 10 weeks onwards.
One thing worth noting: NIPT-based tests do not include an ultrasound scan as part of the test itself. If you would like an ultrasound alongside your NIPT, this can be arranged separately with your doctor.
(To learn more about what the different NICC package tiers cover, please check out our packages)
A Simple Side-by-Side Comparison
| Basic NICC | NIPT-Based NICC | |
| Technology | NT ultrasound + two blood hormone markers (Free Beta-hCG and PAPP-A) | Direct analysis of cell-free fetal DNA from mother’s blood |
| What It Measures | Indirect risk markers (hormone levels and ultrasound measurement) | Baby’s actual DNA fragments circulating in mother’s bloodstream |
| Down Syndrome Detection Rate | Approximately 85 to 90% | Over 99% |
| Result Type | Risk score (for example, 1 in 1,500) | High risk or low risk based on direct DNA analysis |
| Earliest Gestational Age | 11 weeks (must be done by 13 weeks 6 days) | From 10 weeks onwards |
| Conditions Screened | Trisomy 21, 18, and 13 | Trisomy conditions, sex chromosome abnormalities, microdeletions, and more |
| Gender Identification | Not available | Available |
| Includes Ultrasound | Yes, NT scan included | Not included in test (can be arranged separately) |
So Which Test Is Right for You?
We want to be honest with you here. There is no single right answer that fits every pregnancy. The best choice depends on your gestational age, your medical history, your personal circumstances, and what level of reassurance matters most to you.Here is a simple way to think through it.
The Basic NICC may be appropriate if you are between 11 and 13 weeks of pregnancy, you want the NT ultrasound included as part of your screening, and you understand that the result will be a risk estimate rather than a direct DNA finding. It is a well-established, clinically recognised approach that has guided prenatal care for many years.
NIPT-based NICC packages may be more suitable if you want the highest possible accuracy from a DNA-based result, you are at least 10 weeks pregnant, you want to know your baby’s gender, you are 35 years of age or older, you have had a previous pregnancy affected by chromosomal conditions, or you have a family history of genetic disorders.
Something worth considering: If your Basic NICC comes back as high risk, your doctor will likely recommend either a NIPT-based test or an invasive diagnostic test for further clarification. Some mothers, particularly those who find waiting difficult or who have specific risk factors, choose to start with a NIPT-based package directly to avoid the uncertainty of an intermediate result.
There is no wrong choice here. What matters is that you make an informed decision with full understanding of what each approach involves. That is exactly what our doctor at Klinik Caring is here to help you with.
What About Invasive Testing?
You may have heard of amniocentesis or chorionic villus sampling (CVS). It is worth understanding where these fit in.Invasive tests are diagnostic, not screening. They provide a definitive answer rather than a risk estimate. However, they involve inserting a needle into the womb to collect a sample of amniotic fluid or placental tissue. This carries a small but real risk of miscarriage, estimated at approximately 0.5 to 1%.
For this reason, invasive testing is generally only recommended in specific situations: when a screening result has returned high risk, when there is a known family history of a chromosomal condition, or when other clinical factors suggest elevated risk.
Think of NICC screening as your first step. For the vast majority of mothers, results will be reassuring and invasive testing will never be needed. But when a screening result raises concern, knowing that next steps exist and that your doctor will guide you through them calmly is something we hope brings you comfort.
Why Mothers from Singapore Choose Klinik Caring in Johor Bahru
We see many mothers who travel from Singapore specifically for their NICC or NIPT testing at our clinic in Johor Bahru. Here is what they tell us matters most to them.Female doctor: Our clinic is led by a female physician. For many mothers, especially when it comes to pregnancy and sensitive women’s health matters, having a female doctor makes a real difference to how comfortable and safe they feel. This is one of the most common reasons patients tell us they chose Klinik Caring.
We explain, not just report: Receiving a test result without proper explanation can be frightening, especially if the numbers mean nothing to you. At Klinik Caring, our doctor goes through your results with you in plain language, answers every question you have, and makes sure you leave the consultation feeling informed rather than anxious.
Full range of options under one roof: From the Basic NICC to the most comprehensive NIPT-based packages, everything is available at our clinic. You do not need to visit multiple specialists or hospitals to access different levels of screening.
Convenient location for Singapore patients: Our clinic is located in Impian Emas, Skudai, Johor Bahru, which is easily accessible from the Johor-Singapore Causeway. Many Singapore patients find this a practical and comfortable option for their prenatal care needs.
A clinic built on education: Our philosophy at Klinik Caring is “Medicate some days. Educate always.” We believe that an informed mother is an empowered mother. Every consultation is an opportunity to help you understand your health and your baby’s health more deeply.
Frequently Asked Questions
Q: Is NIPT the same as NICC?A: Not exactly. NIPT is an internationally recognised term for cell-free fetal DNA prenatal testing. NICC is Klinik Caring’s prenatal screening programme, which includes both Basic (combined first trimester screening) and higher-tier packages that use NIPT technology. So the Standard NICC and above are NIPT-based, but the Basic NICC is not.
Q: Can NIPT or NICC give a definitive diagnosis of Down Syndrome?
A: No. Both are screening tests, not diagnostic tests. They provide a risk assessment, not a confirmed diagnosis. If results indicate high risk, your doctor will discuss further diagnostic options such as amniocentesis. That said, NIPT-based packages have a detection rate of over 99% for Down Syndrome, making them highly reliable as a screening tool.
Q: I am 9 weeks pregnant. Can I do the test now?
A: For NIPT-based packages, the recommended starting point is 10 weeks. For the Basic NICC, the window is 11 to 13 weeks. If you are 9 weeks today, you may wish to wait just one more week before coming in. Contact us via WhatsApp and we will help you plan the best timing.
Q: I am 35 years old. Does that mean I must do NIPT?
A: There is no strict requirement. However, the risk of chromosomal conditions does increase with maternal age, and many mothers aged 35 and above choose NIPT-based packages for the higher accuracy and broader coverage it provides. Your doctor will help you assess what is appropriate for your individual situation.
Q: I am travelling from Singapore. Do I need to book in advance?
A: Yes, we strongly recommend booking in advance via WhatsApp at 013-943 3314. This ensures our doctor is ready for your consultation and all necessary arrangements for your test are prepared before you make the trip.
Q: What happens after I receive my results?
A: Our doctor will review your results with you in detail during your consultation. For low-risk results, you will receive clear reassurance and guidance for your ongoing pregnancy care. For high-risk results, our doctor will explain your options clearly and support you through the next steps in a calm and caring manner. You will never be left to figure it out alone.
When Should You See a Doctor?
If you are currently pregnant, the most important thing is not to wait too long.For the Basic NICC, the NT ultrasound window closes at 13 weeks and 6 days. Once that window passes, this particular screening option is no longer available.
For NIPT-based NICC packages, testing can begin from 10 weeks. The earlier you test, the more time you have to receive results, process the information, and take any necessary next steps.
Our honest advice: as soon as your pregnancy is confirmed, make an appointment to discuss your prenatal screening options. Even if you are still in the very early weeks, a brief consultation can help you plan ahead with confidence.
If you are unsure which test is right for you, that is exactly what our doctor at Klinik Caring is here for.
Book a Consultation at Klinik Caring, Johor Bahru
We understand that choosing the right prenatal screening can feel overwhelming, especially when you are already navigating the emotional and physical demands of early pregnancy. You do not have to figure it all out on your own.At Klinik Caring in Impian Emas, Skudai, Johor Bahru, our female doctor will sit with you, listen to your concerns, explain your options clearly, and help you make a decision that feels right for you and your baby.
Whether you are from Johor Bahru, Skudai, Nusajaya, or travelling from Singapore, we welcome you.
WhatsApp us today to book your appointment:
📱 013-943 3314
📍 No. 16-01, Jalan Bukit Impian 18/5, Taman Impian Emas, 81300 Skudai, Johor
🌐 www.klinikcaring.com
Mar 13,2026