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NON-INVASIVE PRENATAL TEST
Your Baby's Health is Everything. Trust Europe's Leading NIPT for Unparalleled Peace of Mind
Disponibili tutta l’estate, anche a Ferragosto.
Available nationwide in the Philippines. Home blood collection in the comfort of your own home, with specialized nurses.
Results are available within 7-10 working days from the moment the sample arrives at our state-of-the-art laboratory in Europe.
The test detects the most common trisomies with over 99.9% accuracy, including Down syndrome.
Reliable: The GenePlanet laboratory has performed more than 300.000 test. Highest number of NIPT tests in Europe.
Non-invasive: 100% safe for you and your baby.
We offer a ₱19,500 subsidy to help with confirmatory testing when needed.
Experience:
Advanced Next-Generation Sequencing (NGS) technology with 15+ years of expertise
Advanced Next-Generation Sequencing (NGS) technology with 15+ years of expertise
Risk-Free:
We offer a ₱19,500 subsidy to help with confirmatory testing when needed..
We offer a ₱19,500 subsidy to help with confirmatory testing when needed..
Discreet:
We value your privacy. Your test results are protected by Europe's GDPR - the strictest privacy law
We value your privacy. Your test results are protected by Europe's GDPR - the strictest privacy law
Comprehensive Options
Four distinct packages to fit your needs
Four distinct packages to fit your needs
Find the Best Solution for You
Safe. Early. Reliable. Personalized for Your Needs.
Disponibili tutta l’estate, anche a Ferragosto.
Basic
₱22,000
₱17,600
✨Use code hello2026 ✨
Non invasivo e completamente sicuro per mamma e bambino
📅 Eseguibile dalla 10ª settimana di gravidanza
Analyzes the 3 most common trisomies::
- Down syndrome (Trisomy 21)
- Edwards syndrome (Trisomy 18)
- Patau syndrome (Trisomy 13)
Over 99% accuracy
Gender information**
Standard
₱27,500
₱22,000
✨Use code hello2026✨
Non invasivo e completamente sicuro per mamma e bambino
📅 Eseguibile dalla 10ª settimana di gravidanza
Most common trisomies:
- Down syndrome (Trisomy 21)
- Edwards syndrome (Trisomy 18)
- Patau syndrome (Trisomy 13)
Sex chromosome aneuploidies:
- Turner syndrome (Monosomy X)
- Klinefelter syndrome (XXY)
- Triple X syndrome (XXX)
- Jacobs syndrome (XYY)
Gender information**
Pro
₱40,000
₱32,000
✨Use code hello2026✨
Non invasivo e completamente sicuro per mamma e bambino
📅 Eseguibile dalla 10ª settimana di gravidanza
Most common trisomies:
- Down syndrome (Trisomy 21)
- Edwards syndrome (Trisomy 18)
- Patau syndrome (Trisomy 13)
- Sex chromosome aneuploidies
Additional trisomies:
- Trisomy 9
- Trisomy 16
- Trisomy 22
Sex chromosome aneuploidies:
- Turner syndrome (Monosomy X)
- Klinefelter syndrome (XXY)
- Triple X syndrome (XXX)
- Jacobs syndrome (XYY)
Deletion and duplication syndromes*:
Incidental findings
Gender information**
new
Premium
₱93,000
₱74,400
✨Use code hello2026✨
Non invasivo e completamente sicuro per mamma e bambino
📅 Eseguibile dalla 10ª settimana di gravidanza
Most common trisomies:
- Down syndrome (Trisomy 21)
- Edwards syndrome (Trisomy 18)
- Patau syndrome (Trisomy 13)
- Trisomie 9, 16 e 22
- Anomalie dei cromosomi sessuali
Additional trisomies
- Trisomy 9
- Trisomy 16
- Trisomy 22
Sex chromosome aneuploidies:
- Turner syndrome (Monosomy X)
- Klinefelter syndrome (XXY)
- Triple X syndrome (XXX)
- Jacobs syndrome (XYY)
Deletion and duplication syndromes*:
Incidental findings
Monogenic conditions:
Gender information**
Over 300,000 pregnant women have placed their trust in us.
The highest number of NIPT tests performed in Europe.
Ale Ramírez
Desde que supimos que estábamos esperando un segundo bebé queríamos saber lo más pronto posible que nuestro bebé estuviera sano y mi embarazo en orden, ya que tengo 37 años. Al saber que existía este estudio no dudamos en contactarnos con GenePlanet y realizarlo. Nos dio mucha tranquilidad ver que todos nuestros doctores lo recomiendan. Solicitamos hacer la prueba NIPT by GenePlanet a domicilio. El proceso es súper rápido y fácil de hacer, solo con una muestra de sangre y nos dieron los resultados dos semanas después. Gracias a Dios nuestro bebé viene sano, uno de los beneficios es que te dan la opción de conocer el sexo de tu bebé desde la semana 10 pero nosotros preferimos esperar y no saberlo. Tanto mi esposo como yo, nos sentimos muy tranquilos y felices.
Jessica Arrambide
Gracias a GenePlanet porqué con su estudio NIPT supimos el sexo con mucha anticipación y además porque gracias a los resultados estamos tranquilos que baby viene sano.
Sofía Blanchet
Estar embarazada está siendo la experiencia más maravillosa que he vivido, y lo que más deseamos y anhelamos es que nuestro bebé venga sanito. Por eso no dudé ni un segundo en hacerme la prueba NIPT by GenePlanet y transitar por mi embarazo en paz. Es una prueba no invasiva que con tan solo una muestra de sangre materna te da la confianza de que tu bebé no tiene ningún síndrome, descarta más de 70 y tiene una tasa de detección del 99%. A demás, también te confirma el sexo de tu bebé. ¡Gracias a Dios nuestro bebé viene sano! Después de esta maravillosa noticia vamos a poder seguir gozando de este momento tan mágico que nos regala la vida.
Pau Ortiz
Desde que quedé embarazada, mi vida ha sido una montaña rusa de emociones bonitas, pero es inevitable que entren preocupaciones a la vez al tratarse de una etapa tan importante en la vida. Existen un millón de posibilidades de cosas que pudieran ocurrir o padecimientos que pudiera desarrollar mi bebé, que aunque nada en el mundo puede cambiar el amor tan grande con el que lo esperamos, siempre es reconfortante saber que todo va bien con su desarrollo. Por eso decidí que realizarme la prueba NIPT era una forma de llevar mi embarazo con más paz. Al recibir mis resultados y enterarme que todo va en orden, sentí mucha tranquilidad. Por ello recomiendo que si eres una mujer embarazada en busca de conocer más sobre como va el desarrollo de su bebé, te realices la prueba ¡sin pensarlo dos veces!
Zuly Trevino
Estoy feliz con la prueba prenatal no invasiva que me realice de NIPT by GenePlanet. Me dio mucha tranquilidad y paz saber que todo estaba bien genéticamente en mi bebe. Me encanta saber lo avanzado que estamos cada vez más en la medicina y genética ya que desde muy temprana edad de el embarazo podemos conocer mucho sobre su salud. Feliz con el servicio y atención, 100% recomendado.
Susy Quevedo
Soy Susy Quevedo, mamá de tres, este último embarazo nos llegó por sorpresa y nos tiene muy emocionados. Decidí hacerme la prueba NIPT al igual que en mi embarazo anterior ya que desde la semana 10 podemos obtener toda la información sobre mi bebé, sexo y confirmar que todo venga bien. Nos da la seguridad que buscamos, ya que arroja información que no se ve en el eco ni en las pruebas tradicionales, sin ningún riesgo para mi o para el bebé. Mi ginecólogo estuvo muy a favor de hacernos la prueba y pudimos realizarla en su consultorio. Yo en lo personal recomiendo la prueba a todas las futuras mamás que deseen estar más tranquilas con la salud de su bebé.
Cynthia de la Vega
Este es mi segundo embarazo, y la verdad es que ha sido todo lo contrario al primero. Un sube y baja de noticias y emociones.A diferencia de mi primer embarazo que fue totalmente normal, mi embarazo actual es de alto riesgo en el que por indicación del médico, no debo ni levantarme de la cama. Con más motivo decidí hacerme la prueba NIPT más completa, ya que aunque el doctor me asegura que todo esta en orden, por ser embarazo de alto riesgo pueden pasarte mil cosas por la cabeza, y para mí no hay nada como estar tranquila.La toma de muestra fue super rápida y gracias a que tienen disponible servicio de toma a domicilio me pude hacer la prueba sin tener que salir de cama.Con lo que no contábamos, es que desde la semana 14 de embarazo, con los examenes de primer trimestre, nos enteramos de que iba a ser Niña. Me hice la prueba NIPT en la semana 17 y para la semana 18 nos llegó el resultado más inesperado y hermoso, con la noticia de que ¡será Niño! El mismo día que recibimos el resultado, quisimos confirmarlo, y efectivamente era Niño.Claro que nos tomó por sorpresa y no podemos estar más que agradecidos y felices de que todos los análisis salieron en orden, esperamos con toda la tranquilidad y seguridad a nuestro nuevo principe.Gracias a GenePlanet por haber formado parte de esta historia, y darme paz durante otro embarazo más.
Dra. Alejandra Finol
Al darles a conocer la prueba NIPT a mis pacientes, también les estoy ofreciendo la tranquilidad de tener más información sobre el estado de su bebé. Con solo una muestra de 10 ml de su sangre (Sangre de la mamá), se pueden estudiar células fetales y detectar riesgos de alteraciones de cromosomas, por ejemplo Síndrome de Down, con muy alta sensibilidad. Es importante que los padres tengan la asesoría correcta en cuanto a la capacidad de la prueba y para eso estamos los médicos para guiarlos y darles las opciones con las que contamos. Sin duda, seguiré recomendando esta prueba a mis pacientes, sobretodo a aquellas con antecedentes o con 35 años o más.
Dr. Victor Manuel Carlos Martínez
Recomiendo ampliamente La prueba NIPT by GenePlanet, me dedico 100% al diagnóstico prenatal para mis pacientes y para mi es de gran ayuda tener a nuestro alcance esta prueba con una sensibilidad tan alta y con la gran ventaja de ser no invasiva. Estrés, ansiedad, depresión y muchas dudas surgen cuando a los bebes se les observa un marcador relacionado a un síndrome o una malformación mayor, respecto a que es a lo que realmente nos enfrentamos, en lo personal me deja tranquilo el saber que la sensibilidad para la detección de estas alteraciones es muy alta con NIPT by GenePlanet y esa misma tranquilidad y confianza se la puedo otorgar a los padres, ya hemos realizado bastantes pruebas y puedo decir que los resultados son sumamente confiables y corroborados.
Dr. César Rodolfo Tawney Serrano
En medicina Materno Fetal, nos especializamos en evaluar la salud de mamá y bebé. Durante el embarazo una de las principales dudas de los papás es conocer el bienestar de su bebé. Es por ello que durante el control prenatal el primer estudio avanzado se realiza en la semana 11-13.6 (3 meses) y se complementa con NIPT By GenePlanet para detectar de forma temprana alteraciones anatómicas y condiciones genéticas creando así una amalgama perfecta para tú tranquilidad, con una tasa de detección de hasta 99 %
Are you pregnant? Become a GenePlanet NIPT Ambassador!
✨ What's in it for you?
✅ The most comprehensive NIPT test on the market
🎁 Carefully selected gifts
🧬 Access to our complete range of DNA tests
💡 You're the right person if:
✔️ You're planning to take (or have just taken) the NIPT test
✔️ You have an active social media presence (10K followers)
✔️ Your content reflects our values
Why Choose the NIPT Test?
This non-invasive prenatal screening is simple, safe, and highly accurate, and is designed to provide helpful information about your baby’s genetic profile. Using advanced laboratory technologies, NIPT by Geneplanet evaluates chromosomal information to identify variations that may be present.
The screening provides insight into the likelihood of certain chromosomal variations, including those commonly screened for during pregnancy, as well as many others, regardless of maternal age.
By offering information early in pregnancy, this screening supports expectant parents in making informed choices about prenatal care in consultation with their healthcare provider and planning ahead with greater confidence. Many women choose to include prenatal screening as part of their overall pregnancy care, and NIPT by Geneplanet is recognized as a comprehensive and reliable screening option.
Its performance has been evaluated in large-scale clinical research involving more than 147,000 pregnancies.
Learn more about your baby’s genetic profile with a non-invasive prenatal screening designed to provide reliable information during pregnancy
Choose a high-precision screening option to support peace of mind as you plan your prenatal care. Contact us today to learn more.
Choose a high-precision screening option to support peace of mind as you plan your prenatal care. Contact us today to learn more.
Quick Access Throughout the Philippines
Our partners offer convenient access to the test at convenient locations. Your blood sample will be collected by a qualified professional. The blood draw can be performed directly at your home, at no additional cost
+63 91 7811 9280
Most pregnant women have an appointment scheduled within the same week. If you need an immediate appointment, please call us: we'll schedule it as soon as possible (even within 3 days of your call).
Disponibili tutta l’estate, anche a Ferragosto.
Why is NIPT by GenePlanet the Most Reliable Non-Invasive Prenatal Test?
How Does the NIPT Test Work?
The NIPT test requires only a small 10 ml blood sample taken from your arm. During pregnancy, small amounts of your baby’s genetic material naturally circulate in the mother’s blood. From around the 10th week of pregnancy, there is usually enough of this information to allow a prenatal screening to be done safely and easily through a simple blood sample.
Often chosen as a more advanced screening option compared to traditional prenatal screenings, such as ultrasound-based checks.
Compared with traditional prenatal screening methods, such as ultrasound-based checks, NIPT is widely recognized for providing more detailed screening information and for reducing the likelihood of unclear or misleading results. Because of this, many women are less likely to be referred for follow-up procedures that may not be necessary.
In many healthcare settings, the introduction of NIPT has helped reduce the overall use of invasive follow-up testing by providing clearer screening insights earlier in pregnancy.
Nuchal translucency screening is only about 80% accurate in detecting chromosomal abnormalities. This means that out of 100 women carrying a baby with Down syndrome, nuchal translucency screening will correctly identify only around 80 cases, while NIPT has an accuracy rate of over 99%.
Safer than amniocentesis
Compared with amniocentesis, which is a commonly used prenatal diagnostic procedure, NIPT is a non-invasive screening option. Because it does not involve invasive steps, it is generally chosen to provide screening information without adding physical risk during pregnancy. For this reason, many women consider NIPT as part of their overall prenatal care in consultation with their healthcare provider.
You Can Count on Us.
You can contact our experts at any time - they will resolve any doubts and answer your questions.
Free genetic counseling exclusively with a clinical genetics specialist.
If screening results indicate a higher level of concern, the costs of follow-up procedures, such as amniocentesis or chorionic villus sampling, are covered by GenePlanet. The expectant mother, in consultation with her doctor, may choose the clinic or medical facility where the procedure will be performed.
An additional benefit is complimentary consultation with a clinical genetic specialist, who will help explain the screening results, answer questions, and provide guidance on possible next steps.
Is NIPT Right for Me?
The American College of Obstetricians and Gynecologists (ACOG) published guidelines titled “Screening for Fetal Chromosomal Abnormalities” (October 2020), recommending that all pregnant women be offered NIPT. The guidelines highlight NIPT as the prenatal screening method with the highest sensitivity and specificity.
NIPT is suitable for any woman who:
wants to enjoy peace of mind and a sense of security during pregnancy,
- has a family history of chromosomal defects,
- received high-risk results from other first-trimester screening tests,
- is 35 years old or older, which significantly increases the risk of Down syndrome. However, most other chromosomal abnormalities can occur regardless of the mother's age.
NIPT is also suitable for in vitro pregnancies and twin pregnancies.
Why choose us?
NIPT by GenePlanet is a modern brand that offers one of the most precise prenatal genetic testing services available. Our tests are of the highest quality and provide detailed information about your baby’s genetic health.
GenePlanet, based in Europe, is an international company providing DNA testing services worldwide and is a recognized leader in Europe. We use advanced DNA analysis technologies and work closely with leading experts in the field of genetics to ensure professional testing services and expert consultation.
With our state-of-the-art technology and comprehensive, professional support, we are committed to providing the best possible experience for expectant mothers.
GenePlanet, based in Europe, is an international company providing DNA testing services worldwide and is a recognized leader in Europe. We use advanced DNA analysis technologies and work closely with leading experts in the field of genetics to ensure professional testing services and expert consultation.
With our state-of-the-art technology and comprehensive, professional support, we are committed to providing the best possible experience for expectant mothers.
Frequently Asked Questions FAQ:
NIPT is one of the leading options in prenatal screening. If you have any questions, please refer to the section where we have gathered the most frequently asked questions.
Is this the original NIPT?
GenePlanet is a leading provider of NIPT testing in the European Union, with over 15 years of experience in offering a wide range of DNA testing services across the region.
When can I expect the results?
You'll receive your results within 4-10 business days. 95% of patients receive their results within 7 business days.
Why is our price affordable?
By combining an online booking service with a strong laboratory network, we can focus on testing and provide consultations in the event of high-risk results. Our goal is to make cutting-edge NIPT testing available to as many mothers as possible, so they can enjoy a carefree pregnancy.
Where can I take the NIPT test?
Our team will contact you with the details and arrange an appointment with a selected medical practitioner.
I had a nuchal translucency ultrasound and the results were normal. Is that enough?
The nuchal translucency test (NTT) is an ultrasound that measures the thickness of the fluid layer in the fetal neck fold and calculates the risk of abnormalities. This test's sensitivity is up to 80% for the most common trisomies (Down syndrome, Edwards syndrome, and Patau syndrome), while the NIPT test has a sensitivity of over 99%. The NTT detects only the three most common forms of trisomy, while the NIPT test also detects over 90 other chromosomal abnormalities that may not be visible with ultrasound. However, it is recommended to have both tests, because the NTT can also detect morphological abnormalities that are not necessarily the result of genetic abnormalities and therefore will not be detected by the NIPT test.
How reliable is the NIPT test?
Using advanced genetic screening technology, NIPT provides high-level screening insight for commonly screened chromosomal variations during pregnancy. Its screening performance has been evaluated in large-scale clinical research, making it a widely trusted option in prenatal screening. The screening is designed to offer strong sensitivity for the most commonly screened chromosomal patterns, including those related to chromosomes 21, 18, and 13, as well as sex chromosomes. Screening for other chromosomal changes may vary, as available research data is more limited.If requested, the screening can also provide information about the baby’s sex.
What do the results look like?
NIPT screening results may show a lower or higher level of concern for the chromosomal patterns included in the screening.
A lower-concern result means the screening did not suggest an increased likelihood of the variations being screened, and usually no further testing is recommended unless advised by your doctor. A higher-concern result means your OB-GYN may recommend confirmatory testing, such as amniocentesis or CVS, to provide clearer information.
Your doctor will explain the purpose and considerations of these procedures before you decide. To provide added support, a ₱19,500 subsidy is available to help cover the cost of confirmatory testing when recommended.
The clinic or medical facility can be chosen in consultation with your OB-GYN. A complimentary consultation with a clinical genetics specialist is also included to help explain results and guide next steps.
A lower-concern result means the screening did not suggest an increased likelihood of the variations being screened, and usually no further testing is recommended unless advised by your doctor. A higher-concern result means your OB-GYN may recommend confirmatory testing, such as amniocentesis or CVS, to provide clearer information.
Your doctor will explain the purpose and considerations of these procedures before you decide. To provide added support, a ₱19,500 subsidy is available to help cover the cost of confirmatory testing when recommended.
The clinic or medical facility can be chosen in consultation with your OB-GYN. A complimentary consultation with a clinical genetics specialist is also included to help explain results and guide next steps.
What is the NIPT test?
NIPT is a modern, non-invasive prenatal genetic screening designed to provide information about your baby’s genetic profile. The test requires only a small blood sample from the mother (about 10 ml).During the initial steps of the process, small fragments of the baby’s DNA naturally present in the mother’s blood are carefully separated and analyzed using advanced next-generation sequencing (NGS) technology. This approach allows for detailed and reliable screening without invasive procedures.
How is the NIPT test different from other prenatal tests?
GenePlanet’s NIPT screening is designed with the comfort and safety of both mother and baby in mind and covers a wide range of chromosomal patterns. It is recognized for providing clear screening insights while helping reduce the likelihood of unclear results. As a result, many women may be less likely to need follow-up invasive procedures, in consultation with their healthcare provider.
Is the NIPT test recommended for every pregnant woman?
NIPT screening is an option for all pregnant women. It is often especially considered by women who may have a higher chance of certain genetic variations, based on factors such as maternal age, family medical history, results from other prenatal screenings, or findings from ultrasound examinations.
What information does the NIPT test provide?
The screening allows early identification of a wide range of commonly screened genetic variations, including those related to chromosomes 21, 18, and 13, as well as certain smaller chromosomal changes. NIPT is considered one of the most comprehensive prenatal screening options available during pregnancy.
Does the NIPT test provide information about the baby's gender?
Yes, NIPT screening can also provide information about the baby’s sex early in pregnancy, if requested.
How reliable are the NIPT test results?
NIPT is an updated form of prenatal DNA screening that uses advanced methods to provide detailed screening information during pregnancy. It is designed to offer a high level of screening accuracy. In cases where the screening indicates a possible concern, a healthcare provider may recommend additional confirmatory testing using other medical procedures.
When is it useful to take the NIPT test?
NIPT screening can be considered regardless of a woman’s age or family medical history. By helping screen for commonly tested genetic variations, it supports expectant parents in approaching pregnancy with greater confidence and peace of mind. The screening can be done early in pregnancy, starting from around the 10th week.
How is the test performed??
NIPT screening is designed to be gentle and non-invasive for both the mother and the baby. The process is simple: choose a screening package, schedule an appointment with a doctor, and provide a small blood sample taken from a vein in the arm.Screening results are typically available within 4 to 10 days after the sample is received by the laboratory.
Does the NIPT test detect heart defects?
NIPT screening focuses on identifying specific genetic patterns, such as certain trisomies and smaller chromosomal changes. It is not designed to screen for heart conditions or other structural organ concerns. Imaging tests, such as ultrasound examinations, are commonly used by healthcare providers to check for heart-related or other physical findings during pregnancy.
Is the NIPT test worth it?
NIPT screening offers several benefits. It is non-invasive, designed to provide clear screening insights, and allows early screening for specific genetic patterns. The information may help bring peace of mind or support expectant parents and healthcare providers in planning appropriate prenatal care.
How much does the NIPT test cost?
NIPT screening packages start from €400, with pricing depending on the scope of the selected package. More comprehensive screening options are available at a higher cost. For those who choose more extensive packages, installment payment options may be offered.
Can I get reimbursement for the GenePlanet NIPT test through health insurance?
NIPT screening may be eligible for insurance reimbursement, depending on your provider. A ₱19,500 subsidy is also available to support confirmatory testing when recommended by a doctor.
Can the NIPT test be wrong?
Yes. While NIPT screening is designed to provide highly accurate screening information, no screening test is completely accurate. There is a small possibility that results may suggest a concern that is not confirmed, or may not identify a variation that is present.For this reason, NIPT screening results should always be considered together with overall risk factors and discussed with a healthcare provider. When needed, additional diagnostic methods may be recommended for confirmation.
Which is better – amniocentesis or NIPT?
NIPT screening is non-invasive and is designed to involve a lower level of risk during pregnancy. Amniocentesis, on the other hand, is a more invasive procedure and may involve a higher chance of complications. However, it can provide more definitive diagnostic information.When NIPT screening results do not indicate increased concern, it may help many women avoid invasive testing. The choice of which test to use should always be made in consultation with a healthcare provider, who can advise based on individual circumstances.
What does the NIPT test detect?
The NIPT test by Geneplanet is the most comprehensive NIPT test on the market, covering a variety of conditions: all chromosomal aneuploidies and over 92 microdeletions and microduplications, including incidental findings greater than 5Mbp.
The most common chromosomal syndromes that are screened for by the NIPT test:
Down Syndrome (Trisomy 21)
Incidence: Down syndrome occurs in approximately 1 out of every 700 live births.
Common Characteristics: People with Down syndrome may experience a range of physical and developmental differences. These can include learning challenges, distinct facial features, lower muscle tone, congenital heart conditions, hearing challenges, and developmental delays. The type and level of support needed can vary from person to person.
Living with Down Syndrome: Individuals with Down syndrome have a wide range of abilities and may require different levels of support throughout their lives. There may also be an increased likelihood of certain health conditions, such as respiratory infections, thyroid-related concerns, and early-onset Alzheimer’s disease. With appropriate medical care, early support, and inclusive environments, many individuals lead fulfilling lives.
Additional Information: Down syndrome is a genetic condition caused by an extra copy of chromosome 21. It is often identified during pregnancy or shortly after birth. Early support and appropriate care can play an important role in improving overall quality of life.
Common Characteristics: People with Down syndrome may experience a range of physical and developmental differences. These can include learning challenges, distinct facial features, lower muscle tone, congenital heart conditions, hearing challenges, and developmental delays. The type and level of support needed can vary from person to person.
Living with Down Syndrome: Individuals with Down syndrome have a wide range of abilities and may require different levels of support throughout their lives. There may also be an increased likelihood of certain health conditions, such as respiratory infections, thyroid-related concerns, and early-onset Alzheimer’s disease. With appropriate medical care, early support, and inclusive environments, many individuals lead fulfilling lives.
Additional Information: Down syndrome is a genetic condition caused by an extra copy of chromosome 21. It is often identified during pregnancy or shortly after birth. Early support and appropriate care can play an important role in improving overall quality of life.
Edwards Syndrome (Trisomy 18)
Incidence: 1 in 5,000 live births
Most common symptoms: severe intellectual disability, microcephaly, clenched fists with overlapping fingers, heart defects, organ defects, and developmental delays.
Vivere con la sindrome di Edwards: Edwards syndrome is a serious condition, and many affected infants do not survive beyond the first year of life. Those who survive may have significant intellectual and physical disabilities and will require specialized medical care.
Further information: Edwards syndrome is caused by an extra copy of chromosome 18. It is usually diagnosed during pregnancy or shortly after birth. Treatment for Edwards syndrome consists of supportive care and focuses on improving quality of life.
Most common symptoms: severe intellectual disability, microcephaly, clenched fists with overlapping fingers, heart defects, organ defects, and developmental delays.
Vivere con la sindrome di Edwards: Edwards syndrome is a serious condition, and many affected infants do not survive beyond the first year of life. Those who survive may have significant intellectual and physical disabilities and will require specialized medical care.
Further information: Edwards syndrome is caused by an extra copy of chromosome 18. It is usually diagnosed during pregnancy or shortly after birth. Treatment for Edwards syndrome consists of supportive care and focuses on improving quality of life.
Patau Syndrome (Trisomy 13)
Incidence: 1 in 10,000 live births.
Most common symptoms: severe intellectual disability, cleft lip/palate, eye abnormalities, extra fingers and toes, heart defects, and organ defects.
Living with Patau syndrome: Patau syndrome is a serious condition, and many affected infants do not survive their first year of life. Those who survive may have significant intellectual and physical disabilities and will require specialized medical care.
More information: Patau syndrome is a genetic disorder caused by an extra copy of chromosome 13. It is usually diagnosed during pregnancy or shortly after birth. Treatment for Patau syndrome is individualized to the patient, with supportive care and improved quality of life.
Most common symptoms: severe intellectual disability, cleft lip/palate, eye abnormalities, extra fingers and toes, heart defects, and organ defects.
Living with Patau syndrome: Patau syndrome is a serious condition, and many affected infants do not survive their first year of life. Those who survive may have significant intellectual and physical disabilities and will require specialized medical care.
More information: Patau syndrome is a genetic disorder caused by an extra copy of chromosome 13. It is usually diagnosed during pregnancy or shortly after birth. Treatment for Patau syndrome is individualized to the patient, with supportive care and improved quality of life.
Turner Syndrome (Monosomy X)
Incidence: 1 in 2,500 live female births
Most common symptoms: short stature, infertility, heart defects, kidney abnormalities, and developmental delays.
Living with Turner syndrome: Turner syndrome is a genetic disorder that affects only women and can cause a wide range of symptoms that vary greatly among affected individuals. Hormone replacement therapy and other supportive measures can help manage symptoms and improve quality of life.
Learn more: Turner syndrome is caused by the absence of a complete or partial copy of the X chromosome in females. It is usually diagnosed in childhood or adolescence. Early diagnosis and timely treatment can significantly improve outcomes for people with Turner syndrome.
Most common symptoms: short stature, infertility, heart defects, kidney abnormalities, and developmental delays.
Living with Turner syndrome: Turner syndrome is a genetic disorder that affects only women and can cause a wide range of symptoms that vary greatly among affected individuals. Hormone replacement therapy and other supportive measures can help manage symptoms and improve quality of life.
Learn more: Turner syndrome is caused by the absence of a complete or partial copy of the X chromosome in females. It is usually diagnosed in childhood or adolescence. Early diagnosis and timely treatment can significantly improve outcomes for people with Turner syndrome.
Klinefelter syndrome (47,XXY)
Incidenza: 1 su 500 nascite maschili vive
Most common symptoms: small testicles, infertility, tall stature, gynecomastia (breast enlargement), and developmental delays.
Living with Klinefelter syndrome: Klinefelter syndrome is a genetic disorder that affects men and causes a wide range of symptoms that vary widely among affected individuals. Hormone replacement therapy and other supportive measures can help manage symptoms and improve quality of life.
Additional information: Klinefelter syndrome is caused by the presence of an extra X chromosome in males, with a karyotype of 47,XXY. The syndrome is usually diagnosed during adolescence or adulthood. Early diagnosis and timely treatment can significantly improve outcomes for people with Klinefelter syndrome.
Most common symptoms: small testicles, infertility, tall stature, gynecomastia (breast enlargement), and developmental delays.
Living with Klinefelter syndrome: Klinefelter syndrome is a genetic disorder that affects men and causes a wide range of symptoms that vary widely among affected individuals. Hormone replacement therapy and other supportive measures can help manage symptoms and improve quality of life.
Additional information: Klinefelter syndrome is caused by the presence of an extra X chromosome in males, with a karyotype of 47,XXY. The syndrome is usually diagnosed during adolescence or adulthood. Early diagnosis and timely treatment can significantly improve outcomes for people with Klinefelter syndrome.
DiGeorge Syndrome (22q11.2 Deletion Syndrome)
Incidence: 1 in 4,000 live births
Common symptoms: heart defects, cleft palate, immune system deficiencies, facial abnormalities, developmental delays, learning disabilities.
Living with DiGeorge syndrome: Some signs and symptoms may be visible at birth, while others may not appear until later in infancy or early childhood. People with DiGeorge syndrome are also at increased risk of developing autoimmune disorders and psychiatric disorders, including schizophrenia and anxiety disorders.
Learn more: DiGeorge syndrome is a genetic disorder caused by a deletion of a small fragment of chromosome 22. It has a wide range of symptoms, which can vary greatly among affected individuals. In most cases, DiGeorge syndrome is a "de novo" event; only about 10% of cases are inherited from a parent..
Common symptoms: heart defects, cleft palate, immune system deficiencies, facial abnormalities, developmental delays, learning disabilities.
Living with DiGeorge syndrome: Some signs and symptoms may be visible at birth, while others may not appear until later in infancy or early childhood. People with DiGeorge syndrome are also at increased risk of developing autoimmune disorders and psychiatric disorders, including schizophrenia and anxiety disorders.
Learn more: DiGeorge syndrome is a genetic disorder caused by a deletion of a small fragment of chromosome 22. It has a wide range of symptoms, which can vary greatly among affected individuals. In most cases, DiGeorge syndrome is a "de novo" event; only about 10% of cases are inherited from a parent..
The NIPT test can also detect the baby's sex on demand.
The NIPT test is 99.53% reliable in detecting the baby's sex starting from the 10th week of pregnancy.
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NIPT test by Geneplanet – non-invasive prenatal test. Millions of women have used it!
NIPT is one of the tests that allows you to rule out many diseases and genetic defects! It provides reliable results even in the early stages of pregnancy, and at the same time, it carries no risk. It's no coincidence that 10 million women worldwide have already relied on this test!
What is NIPT and how is it different from other prenatal tests?
Compared with other prenatal screening options, NIPT screening is designed to provide results more quickly and with a high level of screening accuracy. While it does not replace other prenatal screenings performed at different stages of pregnancy, it works well as a complement to them. For this reason, it is often considered alongside nuchal translucency measurement, an ultrasound-based examination that helps assess certain physical developments during pregnancy.
NIPT screening is a genetic screening option that can provide information about a wide range of genetic patterns early in pregnancy, starting from around the 10th week. It analyzes small fragments of genetic material naturally present in the mother’s blood, which allows screening without invasive procedures.
Because the screening is done through a simple blood sample, it is non-invasive and avoids the risks and discomfort that may be associated with invasive testing methods.It is also important to note that NIPT differs from other prenatal screening approaches by offering broader screening coverage and a simple testing process, while helping reduce the likelihood of unclear screening results. This may help many expectant parents avoid unnecessary stress and the need for invasive follow-up procedures, in consultation with their healthcare provider.
NIPT screening is a genetic screening option that can provide information about a wide range of genetic patterns early in pregnancy, starting from around the 10th week. It analyzes small fragments of genetic material naturally present in the mother’s blood, which allows screening without invasive procedures.
Because the screening is done through a simple blood sample, it is non-invasive and avoids the risks and discomfort that may be associated with invasive testing methods.It is also important to note that NIPT differs from other prenatal screening approaches by offering broader screening coverage and a simple testing process, while helping reduce the likelihood of unclear screening results. This may help many expectant parents avoid unnecessary stress and the need for invasive follow-up procedures, in consultation with their healthcare provider.
The technology behind the NIPT test
NIPT screening uses advanced genetic analysis methods to examine small fragments of genetic material found naturally in the blood. These fragments, known as cell-free DNA, circulate in the bloodstream during pregnancy and include genetic material from both the mother and the developing baby.
The screening process
The NIPT screening begins with a simple blood sample taken from the pregnant woman’s arm. This can be done as early as the 10th week of pregnancy, although some women choose to have the screening a little later, between the 12th and 14th weeks.
After the sample is collected, it is sent to a laboratory for analysis using advanced sequencing techniques. Screening results are typically available within a few days after the sample is processed.
The screening process
The NIPT screening begins with a simple blood sample taken from the pregnant woman’s arm. This can be done as early as the 10th week of pregnancy, although some women choose to have the screening a little later, between the 12th and 14th weeks.
After the sample is collected, it is sent to a laboratory for analysis using advanced sequencing techniques. Screening results are typically available within a few days after the sample is processed.
What diseases does the NIPT test detect?
The NIPT test can detect many different genetic disorders, including trisomies, which are responsible for Patau syndrome (trisomy 13), Edwards syndrome (trisomy 18), and Down syndrome (trisomy 21).
This test can also identify some of the microdeletions and microduplications that can cause serious disorders in the child. NIPT analysis can identify a wide range of chromosomal abnormalities, including:
- sex chromosome aneuploidies;
- trisomies of chromosomes 9, 16, and 22;
- Turner syndrome, XXX, XYY, and Klinefelter syndrome.
Additionally, the NIPT test result can also include the child's sex..
This test can also identify some of the microdeletions and microduplications that can cause serious disorders in the child. NIPT analysis can identify a wide range of chromosomal abnormalities, including:
- sex chromosome aneuploidies;
- trisomies of chromosomes 9, 16, and 22;
- Turner syndrome, XXX, XYY, and Klinefelter syndrome.
Additionally, the NIPT test result can also include the child's sex..
Test sensitivity and specificity: is it worth taking the test?
The NIPT test is characterized by a very high sensitivity, reaching 99%. This effectiveness has been confirmed by large-scale validation studies involving approximately 147,000 pregnant women. This means that this test can correctly identify almost all cases of trisomy and other genetic diseases. Furthermore, the risk of obtaining a false-negative result is very low (less than 0.01%). Furthermore, the NIPT genetic test has the lowest rate of missed results or the need for retesting.
When is it best to do the NIPT test?
There are no contraindications to this test, especially considering it only involves a blood sample from the elbow. It can be performed by any expectant mother wishing to assess the risk of trisomy and other abnormalities in her baby. This can help dispel any concerns in the early weeks and allow her to enjoy her pregnancy.
This test is especially recommended when:
- the pregnant woman is over 35 years old—with age, the risk of the baby developing trisomy 13, 18, and 21, among other conditions, increases;
- there is a family history of genetic disorders;
- first-trimester screening tests have revealed abnormalities.
This test is especially recommended when:
- the pregnant woman is over 35 years old—with age, the risk of the baby developing trisomy 13, 18, and 21, among other conditions, increases;
- there is a family history of genetic disorders;
- first-trimester screening tests have revealed abnormalities.
NIPT test results
As mentioned above, the NIPT test is a noninvasive test with a 99% certainty. If the result is negative, no invasive tests are necessary. However, abnormal results should be confirmed with amniocentesis. This procedure involves sampling a small amount of amniotic fluid, which contains fetal cells. This is done using a thin needle inserted through the mother's abdomen.
NIPT test – price
For the NIPT test, the price can vary depending on the service package selected. Costs start at around €400, but it's important to remember that the quality and accuracy of the test represent an investment in the future health of the child. Women typically have several packages to choose from, which differ in the scope of the tests performed. The more tests performed, the higher the price.
The NIPT test is a modern and effective prenatal test that allows for the early detection of many genetic diseases. Thanks to this test, expectant parents can make informed decisions about how to proceed with the pregnancy, taking into account the health of their child.
The NIPT test is a modern and effective prenatal test that allows for the early detection of many genetic diseases. Thanks to this test, expectant parents can make informed decisions about how to proceed with the pregnancy, taking into account the health of their child.
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