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The Fetal DNA test in maternal peripheral blood allows us to rule out specific alterations in the baby with a high rate of precision.
The Fetal DNA (or DNA) test in maternal peripheral blood is a non-invasive genetic screening method that allows us to rule out certain alterations in the baby with a high precision rate, including chromosomal disorders such as Down syndrome, Edwards syndrome, or Patau syndrome, among others.
It can be performed from the 10th week of pregnancy.
It is important for the baby to come for the sample collection after fasting for a minimum of 6 hours
No, the fetal DNA test is safe for both you and the baby. There is no risk of harm to the fetus during the test.
Through this test, it is possible to rule out, with a high level of certainty, chromosomal disorders such as Down syndrome (up to 99%), Edwards syndrome (up to 97%), Patau syndrome (up to 96%), and alterations in the baby’s sex chromosomes.
Genetic conditions such as Down syndrome, Edwards syndrome, Patau syndrome, and alterations in the baby’s sex chromosomes.
We take a sample of peripheral venous blood from your forearm through a small puncture. The blood extraction takes less than 10 minutes.
No, it is not an invasive method. We will only take a small blood sample from your arm, which poses no risk to the baby.
You do not need anesthesia for this test. During the blood extraction, you will only feel a slight prick.
Results are usually available between 10 and 14 business days after the sample is taken. Once validated, we will send them to your email and doctor’s.
Gynecologist and Obstetrician with a subspecialty in Maternal Fetal Medicine and training in advanced fetal echocardiography.
Certified by the Mexican Council of Specialists in Gynecology and Obstetrics, and the Fetal Medicine Foundation. As an expert in maternal-fetal health, I try to convey to my patients the importance of care and supervision during pregnancy.
Gynecologist and Obstetrician with a subspecialty in Maternal-Fetal Medicine, certified by the Mexican Council of Specialists in Gynecology and Obstetrics and the Fetal Medicine Foundation.
Expert in the monitoring and management of high-risk pregnancies, detection of congenital disabilities, and twin pregnancies.
Gynecologist and Obstetrician with a subspecialty in Maternal Fetal Medicine by the UNAM. Experienced in the management of high risk obstetric and gynecologic pathology.
Certified by the Fetal Medicine Foundation in Cervical Assessment, Preeclampsia Detection and Doppler Ultrasound. Afiliado a la International Society for Prenatal Diagnosis y The Society for Maternal-Fetal Medicine. Affiliated to the International Society for Prenatal Diagnosis and The Society for Maternal-Fetal Medicine.
It is performed between the 11th and 14th week, and with it, we can know how many weeks of pregnancy you have and if there is a risk of Down Syndrome.
It is a blood test that detects two placental hormones; it improves the detection of Down Syndrome, Preeclampsia, and growth restriction.
During the second trimester, we carefully evaluate your baby's organs.
It provides information about the baby's growth, position, and the state of the placenta and amniotic fluid.
Our equipment offers images of greater clarity and resolution, which allows you to get to know your baby on a deeper level.
Allows for the evaluation of the baby's heart development and function, identifying possible heart anomalies and ensuring appropriate monitoring during pregnancy.
It consists of extracting amniotic fluid by means of an ultrasound-guided needle. It is performed after 15 weeks for the prenatal diagnosis of genetic disorders.
It is a procedure in which a small placenta sample is obtained under ultrasound control. It is performed between 10 and 14 weeks to diagnose genetic diseases.
It is a test that evaluates the behavior of your baby's heart and helps us determine if its oxygen supply is adequate.
It allows you to rule out chromosomal alterations in your baby, such as Down syndrome, using a blood sample from the mother.
Helps to relieve pain and discomfort caused by postural changes during pregnancy, improving lumbopelvic mobility, decreasing circulatory problems and maintaining pelvic floor muscle tone.
Improves musculoskeletal structures after pregnancy, provides lymphatic drainage and treatment for soft tissues and scars, facilitating a healthy and safe recovery.
Personalized nutrition plan to enhance chances of successful pregnancy. Custom strategies for couples diagnosed with infertility. Includes comprehensive assessment, tailored recommendations, and ongoing support.
Stage-specific nutritional strategies throughout pregnancy, with progress monitoring and customized recommendations based on each patient's individual needs.
Professional guidance for successful breastfeeding. Includes nursing techniques, solutions for common challenges, and nutritional recommendations during the lactation period.
Av. Paseo de la Reforma 2654. Torre Quadrata, 14th Floor, Offic. 1401. Lomas Altas. Miguel Hidalgo. Zip Code 11950. CDMX.
