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2026.04.10


The Newborn Postnatal Test by seeDNA Genetic Medical Laboratories is Japan's first genetic testing service targeting postnatal babies to check the risk of chromosomal aneuploidies such as Down syndrome or sex chromosome aneuploidies such as Klinefelter syndrome.
It is widely known that early diagnosis is crucial in treating various diseases. However, some feel resistance to prenatal testing. Even for those, a test equivalent to Prenatal NIPT can be easily taken after the baby is born.
Why not clear your anxieties about your child's genetic conditions with the Newborn Postnatal Test (Postnatal NIPT) by seeDNA Genetic Medical Laboratories?
This is a genetic test that can be taken easily, even for those who had resistance to receiving genetic testing during pregnancy.
It examines the risk of 8 types of chromosomal abnormalities from the sample (oral mucosa) collected by gently rubbing the inside of the baby's cheek with a testing cotton swab.
In addition to syndromes that might be perceived as a genetic individuality rather than a disease due to the lack of conspicuous symptoms, you can understand the risk of genetic conditions that tend to be accompanied by serious complications.
You can perform the test with the same items at 1/3 the cost of Prenatal NIPT.
Accurate

The Newborn Postnatal Test is a clinical research utilizing a patent developed by seeDNA Genetic Medical Laboratories, an ISO9001 certified institution with zero misdiagnosis cases in prenatal DNA parentage testing.
Easy

No hospital visit is required for a blood draw. You can receive the test by mail from any of the 47 prefectures. There is nothing for the customer to prepare, such as referral letters or insurance cards.
Fast

There is no age limit for testing.
Since the sample can be safely collected with an easy method, testing is OK even on the day the baby is born.
You can check the risks of various genetic diseases of your baby in as fast as 3 days.
Safe

In the unlikely event that a serious genetic condition is found, appropriate treatment can be received early.
Even if a test result cannot be obtained due to the condition of the sample, etc., this is a secure test where you can receive a retest with all round-trip shipping costs of the sample collection kit and speed testing fees covered by seeDNA Genetic Medical Laboratories, or receive a partial refund of the testing fee.
* This is not a definitive diagnosis for a disease, but rather a clinical research study to confirm the risks of 8 types of genetic conditions.
In the unlikely event of a result error※1, the test fee will be fully refunded.
※1: If no disease is found in a "high risk" result, or if a disease is found in a "low risk" result.
If results cannot be obtained due to sample transport issues or damage, we will perform a retest free of charge.
With no additional cost, it will be processed as a speed test, allowing you to check the results in 3 to 5 days. No round-trip shipping fee is required.
Not only is the round-trip shipping for the test kit free, but installment and deferred payment fees are also free!
Even if the sample is damaged due to a mailing accident, we will retest free of charge.
By introducing state-of-the-art testing equipment, results are available in as fast as 3 days!
Furthermore, you can have peace of mind as we are a testing institution with zero human errors through automated analysis.
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In the unlikely event of a result error※1, the test fee will be fully refunded.
※1: If no disease is found in a "high risk" result, or if a disease is found in a "low risk" result.
If results cannot be obtained due to sample transport issues or damage, we will perform a retest free of charge.
With no additional cost, it will be processed as a speed test, allowing you to check the results in 3 to 5 days. No round-trip shipping fee is required.
Not only is the round-trip shipping for the test kit free, but installment and deferred payment fees are also free!
Even if the sample is damaged due to a mailing accident, we will retest free of charge.
By introducing state-of-the-art testing equipment, results are available in as fast as 3 days!
Furthermore, you can have peace of mind as we are a testing institution with zero human errors through automated analysis.
In some European countries, over 75% of pregnant women check the risk of genetic diseases in their unborn babies. However, in Japan, due to restrictions on taking tests, high testing costs, and ethical resistance regarding the unborn baby, many women give birth without taking Prenatal NIPT.
With the postnatal NIPT, which is the only one in Japan conducted by seeDNA Genetic Medical Laboratories, the same test as Prenatal NIPT can be easily performed at home.
It also reveals sex chromosome abnormalities such as Klinefelter syndrome and Turner syndrome, which are difficult to identify by appearance alone.
Whether you have received Prenatal NIPT※1 or not, it is important to confirm the health risks of your precious newborn baby. Postnatal NIPT is a genetic testing service that can only be conducted by seeDNA Genetic Medical Laboratories in Japan.
Test results can be confirmed in as fast as 3 days after the sample arrives at our office (Tokyo Lab).
*1: Excludes those who have already received a confirmatory diagnosis such as amniocentesis or chorionic villus sampling.
*2: Submission of a confirmatory diagnosis report and receipt is required. The counseling fee subsidy is limited to once, up to 10,000 yen.
Comparison Table of Newborn Postnatal Test and Prenatal NIPT by seeDNA Genetic Medical Laboratories
| Newborn Postnatal Test | Prenatal NIPT | |
|---|---|---|
| Testing Items | Newborn Postnatal Test ・Down Syndrome (Trisomy 21) ・Edwards Syndrome (Trisomy 18) ・Patau Syndrome (Trisomy 13) ・Turner Syndrome (XO) ・Klinefelter Syndrome (XXY) ・Triple X Syndrome (XXX) ・XYY Syndrome (XYY) ・All Chromosomal Abnormalities (Aneuploidy): Chromosomes 1 to 22 | Prenatal NIPT ・Down Syndrome (Trisomy 21) ・Edwards Syndrome (Trisomy 18) ・Patau Syndrome (Trisomy 13) ・Turner Syndrome (XO) ・Klinefelter Syndrome (XXY) ・Triple X Syndrome (XXX) ・XYY Syndrome (XYY) ・All Chromosomal Abnormalities (Aneuploidy): Chromosomes 1 to 22 ・Gender Test |
| Additional Test | Newborn Postnatal Test × None | Prenatal NIPT Microdeletion |
| Cost | Newborn Postnatal Test 44,800 yen (including tax and round-trip shipping) | Prenatal NIPT 198,000 yen (including tax, round-trip express shipping, and blood draw fee) |
| Speed Testing | Newborn Postnatal Test 3–5 days | Prenatal NIPT × None |
| Regular Testing | Newborn Postnatal Test 7–9 days | Prenatal NIPT 6–8 days |
| Sample | Newborn Postnatal Test Cotton swab rubbed inside the baby's mouth | Prenatal NIPT Maternal blood |
| Clinic Visits | Newborn Postnatal Test None | Prenatal NIPT Once (for blood draw only) |
| Testing Period | Newborn Postnatal Test From the day of birth | Prenatal NIPT Weeks 10 to 16 |
| Age Limit | Newborn Postnatal Test None | Prenatal NIPT None |
| Referral Letter | Newborn Postnatal Test Not required | Prenatal NIPT Not required |
| Confirmatory Diagnosis | Newborn Postnatal Test 50% Subsidy | Prenatal NIPT Full Subsidy |
In the case of genetic conditions caused by chromosomal aneuploidy, early detection and intervention can improve the quality of life in three aspects for both the child and the entire family.
Health Management
Children with genetic conditions such as Down syndrome or Patau syndrome have a higher risk of health issues like heart diseases, hearing or vision problems, and hypothyroidism. Therefore, regular health management by medical experts at hospitals is required.
Education, Rehabilitation & Developmental Support
Besides physical disabilities, special support is often needed in language, motor skills, social abilities, and overall development due to intellectual disabilities. Early detection is important to support development and enhance independence in daily life through early intervention programs. Early educational support contributes to social participation and learning ability improvement, helping children with disabilities maximize their potential.
Family Support
Families raising children with genetic conditions require psychological and social support. Early access to correct information and resources to prepare for child-rearing is crucial for the child's development.
Know the Risk of Genetic Conditions in Unborn Babies

1.Application & Payment


2.Sample Collection

3.Mailing the Sample

4.Receiving Test Results
* The period counts only weekdays, with the day the sample arrives at seeDNA Genetic Medical Laboratories as Day 0.
If the sample arrives in the afternoon, it will be +1 business day.
* The period counts only weekdays, with the day the sample arrives at seeDNA Genetic Medical Laboratories as Day 0.
If the sample arrives in the afternoon, it will be +1 business day.