Non-Invasive Prenatal Testing - NIPT

(8 customer reviews)

NIPT, or non-invasive prenatal testing, is an advanced screening method that uses a simple blood test from the mother to check the baby’s risk of genetic abnormalities. It’s easy, safe, and accurate.
Let Docosan help you navigate this exciting phase of parenthood by providing you with best in class NIPT testing that will empower you to make best decisions for the mom and the baby.

Sample collection method

4,600,000

Know Early & Safely Non-invasive Accurate Results

While a woman is pregnant, small pieces of placental DNA circulate in her bloodstream. This placental DNA Is usually identical to the baby’s DNA.

After 10 weeks gestation, there is enough of this cfDNA, or cell-free DNA, in a pregnant woman’s bloodstream to test for genetic abnormalities in the fetus. Only a simple blood draw from mother is required. Analyzing this cfDNA is an opportunity to detect genetic abnormalities early on without harming the fetus at all.

NIPT is most often used to detect chromosomal disorders such as Down’s Syndrome, Edward’s Syndrome, etc.

HOW IT WORKS

Get customized medical advice and treatment from the comfort of your home, supervised by top doctors across Vietnam

1. Purchase online

Purchase the screening package online using your phone or computer. If you have questions, feel free to chat or call!

2. We’ll call you to schedule a nurse visit

After you purchase, our CS team will reach out to schedule a nurse visit.

3. Results & consultation via the app

Download Docosan’s app and we’ll send your results straight to your phone. You will also receive a free consultation with a licensed doctor on the app based on your results.

4. After-care support

Rest assured that your questions and concerns will be heard, even after you’ve gotten your results and consultation.

WHAT'S MEASURED

Down’s Syndrome – Trisomy 21

Down’s syndrome, also known as trisomy 21, is a genetic disorder caused by the presence of all or part of a third copy of chromosome 21. Down’s syndrome affects 1 in every 700 babies borned each year.

Edward’s Syndrome – Trisomy 18

Edwards’ syndrome, also known as trisomy 18, is a rare but serious condition. Edwards’ syndrome affects how long a baby may survive. It happens to 1 in every 5,000 to 6,000 live births.

Patau’s Syndrome – Trisomy 13

Patau’s syndrome is a serious rare genetic disorder caused by having an additional copy of chromosome 13 in some or all of the body’s cells. It affects 1 in every 5,000 babies borned each year.

Chromosome 1

Chromosome 1 is the largest of the 23 chromosomes. Abnormalities in chromosome 1 can cause intellectual disability, distinctive facial features, physical abnormalities, neurological and psychiatric problems, and some types of cancers, etc.

Chromosome 2

Chromosome 2 is the second largest chromosomes found in human cells. Abnormalities of chromosome 2 cause cancers, intellectual disability, behavioral problems, obesity, and skeletal abnormalities, etc.

Chromosome 3

Chromosome 3 is the third largest chromosomes in humans, which makes up around 7% of the genetic material in the whole genome. Chromosome 3 disorder causes delayed development, intellectual disability, behavioral and psychiatric disorders, and physical abnormalities.

Chromosome 4

Chromosome 4 chromosome represents around 6.5% of the DNA in the human genome and comprises nearly 1000 genes. Abnormalities in Chromosome 4 cause issues like severe intellectual disability and physical abnormalities, and cancers, etc.

Chromosome 5

Chromosome 5 represents almost 6 percent of the total DNA in cells. Some genes on chromosome 5 play important roles in the growth and division of cells. Abnormalities may result in blood disorders, cancers, etc.

Chromosome 6

Chromosome 6 is functionally associated with more than 120 major human diseases, including cancer, heart disease, infectious, immune and inflammatory disorders and mental illnesses.

Chromosome 7

Issues like slow growth, distinctive facial features, delayed development, speech and language problems, and learning disabilitiesare caused by this chromosome abnormalities.

Chromosome 8

Chromosome 8 abnormalities causes health conditions like blood-related cancers, moderate to severe intellectual disability, bone and joint malformations, etc.

Chromosome 9

Bladder cancer, a type of cancer of blood-forming cells called chronic myeloid leukemia, etc. are common issues caused by chromosome 9 abnormalities.

Chromosome 10

Distinctive facial features, growth problems, mild to moderate intellectual disability, developmental delay, genital abnormalities in males, or skeletal or heart defects, and several types of cancer are found in the association with a loss of chromosome 10.

Chromosome 11

Overgrowth, intellectual disability, birth defects and several types of cancers are caused by this chromosomal disorder.

Chromosome 12

Abnormalities involving chromosome 12 are involved in a type of blood cell cancer called PDGFRB-associated chronic eosinophilic leukemia, weak muscle tone, and some types of cancers.

Chromosome 13

Small head size (microcephaly), learning disabilities, slow growth and chromosome-13 related cancers are found associated with this chromosome abnormalities.

Chromosome 14

Intellectual disability, delayed development, brain development disruption, and some types of cancers can be caused by chromosome 14 disorder.

Chromosome 15

Sensorineural deafness, male infertility, intellectual disability, seizures, behavioral problems, autism and psychiatric disorders are associated with chromesome 15 abnormalities.

Chromosome 16

Delayed development, intellectual disability and autism spectrum disorder, the disruption of the development of blood vessels in the lungs are commone issues cased by chromosome 16 disorder.

Chromosome 17

Abnormalities in chromosome 17 can cause loss of sensation, tumor formation, abnormal muscle stiffness, etc.

Chromosome 18

Delayed development and learning disabilities, short stature, weak muscle tone (hypotonia), foot abnormalities are commonly found related to chromosome 18 disorder.

Chromosome 19

Unusually large head size (macrocephaly), tall stature, delayed development of speech and motor skills (such as sitting and walking), intellectual disability, Seizures, feeding and digestive difficulties, and eye abnormalities are common issues related to chromosome 19 abnormalities.

Chromosome 20

Chromosome 20 disorder affects the development of heart, bile ducts in the liver, the spinal column, and certain facial features

Chromosome 21

Production of abnormal, immature white blood cells, Down’s syndrome and some type of cancers are caused by the abnormal chromosome 21.

Chromosome 22

Abnormalities in chromosome 22 can cause heart defects, an opening in the roof of the mouth (a cleft palate), distinctive facial features, low calcium levels, and an increased risk of behavioral problems and mental illness such as schizophrenia; developmental delay, intellectual disability, and absent or severely delayed speech, etc.

Sex-linked chromosomes – X chromosom

The X chromosome represents 5% of the total DNA in women and about 2.5% of the total DNA in men. Mutations in the X chromosomes lead to several genetic disorders like Klinefelter syndrome (sexual development before birth and at puberty), Triple X syndrome (tall stature, developmental delays, learning problems), Turner syndrome (short height, failure of the ovaries to develop and heart defects), etc.

Sex-linked chromosomes – Y chromosome

This chromosomal disorder is a condition that leads to infertility, developmental and behavioral disorders, and other health problems.

STILL HAVE QUESTIONS?

All pregnant women are eligible for NIPT anytime after the 10th week of pregnancy to watch out for abnormalities. There are some groups of women in a higher risk category who are even more strongly encouraged to take this test. You may be high risk if:

  • You are pregnant over 35 years old
    You have abnormal ultrasound results
  • You or the other genetic parent of the baby have a chromosomal disorder
  • You had a previous pregnancy with a chromosomal abnormality

NIPT is a reliable way of determining any abnormalities in your baby. It’s 99% accurate for Down syndrome, 97% for trisomy 18 , and 87% trisomy 13

NIPT is highly accurate, so a positive result is a good indication that further testing and intervention is needed.

Even if the screening test is positive, doctors will request additional, specialized tests to confirm the exact diagnosis.

Don’t worry, Docosan partners with thousands of licensed doctors and hospitals and we are happy to connect you with the right one for further testing if necessary.

For at-home sample collection, we will send a nurse to you. Depending on the location you want, the travel fee can be included in or excluded from the package. Travel fee details are below:

  • District 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, Phú Nhuận, Bình Thạnh, Nhà Bè, Thủ Đức, Bình Chánh (inside Trung Son residential area), Gò Vấp, Tân Phú, Bình Tân, Tân Bình: Included in the package: Nurse fee is included in the package.
  • Bình Chánh(outside Trung Son residential area),Củ Chi, Hóc Môn, Cần Giờ, Bình Dương: 200,000 VND ++ depends on the distance. .

Talk to our medical support team to get the exact fee.

WHY SHOP ON DOCOSAN?

International Standards

Receive the same quality of care as you would in the U.S. or Singapore with standardized treatment algorithms, test kits, and more.

Digital & Convenient

Get all results, and medical advices sent straight to your mobile phone.

Judgement & Stigma-Free

Get sympathetic and dignified care no matter who you are.

Tailored for You

Docosan will always do our best to get you the best care for your need and never sell you unnecessary products.

PEOPLE ALSO BOUGHT

8 reviews for Xét Nghiệm Tiền Sản Không Xâm Lấn – NIPT

Overall experience
100%
Convenience
100%
Value
100%

Reviewed by 08 customer(s)

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  • Avatar

    Mỹ Duyên Nguyễn

    Hợp lí

    1 gói kiểm tra được 23 nhiễm sắc thể luôn. Mà giá cả hợp lí với tôi

    August 5, 2022
  • Avatar

    Linh Dang

    Chi phí hợp lý

    Giá hợp lý hơn các bên khác, xét nghiệm tất cả các NST mà giá gần cả chục triệu. Bạn y tá đến lấy máu nhẹ nhàng, thân thiện. Bác sĩ tư vấn sau xét nghiệm cũng ok lắm.

    August 4, 2022
  • Avatar

    Đào Thị Lan

    Tiện lợi

    Không phải di chuyển đi đâu nhưng vẫn có thể kiểm tra được sức khỏe, chỉ cần tôi đặt là có bác sĩ đến tận nhà để lấy máu, rất tiện lợi

    August 1, 2022
  • Avatar

    Lê Thị Mỹ Hoa

    10 điểm

    Để đảm bảo sức khỏe cho con tôi đã lựa chọn gói này để đảm bảo được sức khỏe của con sau này. Tôi rất thích gói này

    July 25, 2022
  • Avatar

    Hằng Ánh

    Tuyệt vời

    Bác sĩ lấy máu không đau, dặn dò rất kĩ lưỡng, Tuyệt vời

    July 19, 2022

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