Our maternity care packages allow expectant mothers to experience the period leading up to childbirth in safety and serenity. In addition to conducting the most important examinations, we ensure the specific monitoring of the pregnancy, providing specialised care and constant counselling, in order to ensure that they can prepare themselves uninterrupted for the wonderful experiences ahead.

The primary goal of prenatal care is to monitor the health of both the expectant mother and the fetus during pregnancy and to accompany the couple throughout the journey of becoming a family.

Prioritizing the peaceful anticipation of childbirth and the comfort of expectant mothers, laboratory tests, ultrasound examinations, and additional services (exercises, movement therapy, maternity preparation courses, etc. included in the premium package) are all provided in one place, in our tranquil, family-friendly clinics at Maternity Private Clinic.

As a special gift, expecting mothers will receive a complimentary baby movie voucher upon completing the second installment of the prenatal care package.

Our clinic offers choices between BASIC and PREMIUM maternity care packages for expectant mothers.

Ultrasound examinations allow us to monitor the growth and development of the fetus during pregnancy. Through prenatal ultrasound scans, parents can periodically glimpse into the development of the growing fetus. We can get a view on their precise growth in terms of size, hear their heartbeat, check the position of the fetus in the uterus, and detect the quantity of amniotic fluid.

With our modern ultrasound machines, we can capture high-quality images of the developing babies, even during routine ultrasound scans.

The purpose of genetic ultrasound examinations is to detect developmental abnormalities in a timely manner, and to make complications associated with childbirth preventable as soon as possible. Prenatal screening is recommended three times for expectant mothers: around the 12th, 20th, and 30th weeks of pregnancy.

The examination can identify signs of developmental and chromosomal abnormalities, pathological conditions, and any possible placental adhesion disorders.

At our clinic, genetic ultrasound examinations are conducted in two stages with two examiners.  First, a certified and experienced sonographer performs the scan followed by an ultrasound specialist obstetrician-gynecologist who examines the patient. This ensures that our expectant mothers have the most accurate diagnostic procedure available to them.

Fetal echocardiography, which is a detailed examination of the fetal heart performed by a specialist, allows for the identification of congenital heart defects during the fetal phase, and it can be performed with high diagnostic accuracy, as early as the 22nd week of pregnancy.

The examination can help assess various heart conditions, including heart valve, myocardial, and great vessel diseases, in addition to exploring the anatomical conditions of the heart. It can detect numerous developmental abnormalities. Such accurate diagnosis greatly aids in the success of subsequent care. If suspicion of a heart defect is confirmed, we can guide the delivery prepared and planned for such in advance, providing reassurance to our patients.

PROF. KRISZTINA KÁDÁR, PH.D., M.D.

Professor, pediatric cardiologist, pediatrician

Tuesday: 8:00 - 16:00 Thursday: 10:00 - 15:00

Among the diagnostic tests performed during pregnancy, one of the most widespread, in addition to ultrasound examinations, is cardiotocography (CTG), which is essential for monitoring the fetal condition in utero.

The examination is carried out using a specialised instrument that detects changes in fetal heart rate, uterine activity, and fetal movements.

CTG monitoring can be performed at any time from the 24th week of pregnancy, but it is regularly recommended weekly from the 36th week of pregnancy, twice per week from the 38th week, and daily from the 40th week onward. The examination does not cause any pain for either the mother or the baby, making it safe to conduct during pregnancy. Despite its non-invasive nature, it is a very important examination, as it can alert us to numerous fetal conditions or any deterioration in their condition.

Fetal neurosonography is an advanced ultrasound imaging technique specifically designed for the detailed analysis of fetal brain and spinal cord development and structure. Central nervous system abnormalities are the second most common fetal developmental issue after congenital heart defects, making early detection and diagnosis crucial for providing appropriate care.

Why is fetal neurosonography important?

Fetal central nervous system disorders can be of genetic origin, developmental problems, or a result of external influences. The examination helps to:

• Detect developmental abnormalities of the brain and spine,
• Raise early suspicion of genetic-based neurological diseases,
• Assess the possible effects of intrauterine infections,
• Follow-up on previous central nervous system abnormalities in earlier pregnancies.

When is the examination recommended?

The ideal time for the exam is the 26th week of pregnancy, as by this stage, the fetus’s organs are sufficiently developed in terms of structure and size, and the central nervous system is developed enough for a detailed examination, leading to more accurate diagnostics. Due to continuous development, repeat control examinations may also be necessary in the third trimester.

How is the examination performed?

The exam utilizes high-quality 2D, 3D, and specialized 4D ultrasound techniques, enabling detailed visualization of the fetal brain structures and spine. In a cephalic position, both abdominal and vaginal ultrasound probes are used, while in a breech position, the examination is carried out through the upper pole of the uterus.

In which cases is fetal neurosonography particularly recommended?

• For mothers over 35 years old,
• If previous ultrasounds have shown any abnormalities or developmental disorders,
• If there is a family history of hereditary genetic or neurological disorders,
• If the mother has had an infection during pregnancy,
• In the case of twin pregnancies.

What is required before the examination?

• Please bring all relevant documentation related to your pregnancy, including:
• Genetic ultrasound results from the first and second trimesters,
• The results of the combined test,
• The NIPT result (if performed),
• The results of the fetal heart ultrasound and genetic counseling.

What is a baby movie?

A baby movie is a special ultrasound examination during which we can observe the fetus’s facial features, body parts, and movements through 3D and 4D images and videos. With this technology, parents can feel even closer to their unborn child.

What does 4D mean?

4D ultrasound is a modern fetal examination method that displays a three-dimensional image in real-time. This means that the fetus is visible not only as a still image but also in motion, including its facial expressions and ongoing movements.

When is the ideal time for a baby movie?

The most ideal time is between the 25th and 30th week, as the fetus’s size is optimal for the recordings, and there is enough amniotic fluid surrounding the fetus, which helps in making the movements visible.

How long does the baby movie last?

At our clinic, the baby movie examination lasts about 20 minutes, but the duration can be influenced by the fetus’s position. If the fetus is in a good position, the recordings will be completed faster. However, if the fetus is in a less favorable position, more time may be required.

What happens if the fetus is not clearly visible?

It may happen that the fetus is sleeping or has its back turned toward the ultrasound probe. In such cases, we try to wake the fetus up or encourage movement using various techniques. For example, consuming a small amount of chocolate or taking a short walk before the examination may help.

What does the price of the baby movie include?

The price includes a 20-minute video recording of the baby. Additionally, we provide a printed photo as a gift.

The baby movie examinations are performed by our sonographer, Eszter Hozdik.

Traditional biochemical screening

Combined test

The test that can be performed between weeks 11 and 14 of pregnancy is not DNA-based but is intended for risk assessment. It is conducted based on maternal age, ultrasound findings, and markers measured during the blood test. The test is performed in conjunction with the first genetic ultrasound examination. The combined test can also be requested as an additional examination; in this case, its cost will be billed together with the ultrasound examination.

Toxemia screening

The toxemia screening (preeclampsia) can be performed between 11 and 14 weeks of pregnancy and is linked to the first genetic ultrasound examination, which determines the risk of developing pregnancy toxemia in the first trimester. Our prenatal care packages include the combined test and toxemia screening, which are performed between 12 and 13 weeks of pregnancy.

Molecular genetic tests

All genetic tests (NIPT test) are performed in conjunction with an ultrasound examination, which cannot be older than 24 hours. An appointment for the ultrasound examination is required in advance, which can be made online, by phone, or in person at the first-floor reception.

NIPT tests

The NIPT test (Non-Invasive Prenatal Test) is an advanced genetic screening test that can be performed during pregnancy. It measures the risk of fetal genetic disorders using a maternal blood sample.