Antenatal ultrasound scans (low risk and high risk pregnancies)

First Trimester Aneuploidy Screening (Nuchal Translucency NT scan and blood tests)

Second trimester Detailed Organ Scan (Morphology scan)

Third trimester Fetal Growth and Doppler scan

Management of high risk pregnancies

Diagnostic procedures and testing (Chorionic Villus Sampling, Amniocentesis, Non-invasive prenatal test-NIPT)

Pre-conception counselling

Genetic testing

Antenatal ultrasound scans (low risk and high risk pregnancies)

• First Trimester Aneuploidy Screening (Nuchal Translucency scan and blood tests)
  The first-trimester aneuploidy screening, conducted between 11 and 14 weeks of pregnancy, includes a nuchal translucency scan and blood tests. This prenatal assessment aims to assess fetal wellbeing by providing reassurance regarding chromosomal conditions such as Down syndrome, Edward syndrome, and Patau syndrome.Additionally, it helps to accurately determine the pregnancy’s gestational age, identify women at higher risk for developing pre-eclampsia, detect major fetal abnormalities early, and diagnose multiple pregnancies.
• Second trimester Detailed Organ Scan (Morphology scan)
  The second trimester detailed organ scan, known as the morphology scan, is typically performed between 18 and 22 weeks of pregnancy to examine the baby’s organs and structural development comprehensively. This scan checks fetal organs such as the brain, face, spine, heart, stomach, bowel, kidneys, and limbs, although it’s important to note that not all conditions can be detected by ultrasound.Additionally, we evaluate factors like the amount of amniotic fluid, the umbilical cord condition, and the placental position. If the baby’s position allows, we can also attempt to capture 3D/4D images, creating cherished and memorable moments for expecting parents.
• Third trimester Fetal Growth and Doppler scan
  The third trimester Fetal Growth and Doppler scan, is performed between 28 and 33 weeks of pregnancy, focuses on several key assessments. These include monitoring fetal growth, evaluating the placental position, and assessing blood flow to both the placenta and the fetus.
  Additionally, the scan measures the amount of amniotic fluid present and observes the movement of the fetus. This comprehensive evaluation helps ensure the wellbeing of both the mother and the developing baby as the pregnancy progresses.
• Management of high risk pregnanciesOur high risk pregnancy team offers a comprehensive care for the management of complicated pregnancies to ensure the safety and wellbeing of both mother and baby.
  Our services include diagnosis and management of maternal and fetal complications including multiple pregnancies, gestational diabetes, pre-eclampsia, cervical incompetence, premature delivery, blood clotting disorders, congenital anomalies, recurrent pregnancy loss.
• Diagnostic procedures and testingChorionic Villus Sampling (CVS):is recommended for women at higher risk of chromosomal abnormalities during pregnancy or those with a family history of genetic disorders. Typically performed between weeks 11 and 14 of pregnancy, this procedure involves extracting placental tissue for genetic analysis. The tissue sample is then sent to a specialized laboratory to examine the fetal chromosomes and provide diagnostic information.Amniocentesis: is recommended for women at higher risk of chromosomal abnormalities during pregnancy or those with a family history of genetic disorders. Typically performed from 15 weeks of pregnancy onwards, this procedure involves collecting a sample of amniotic fluid. The amniotic fluid sample is then sent to a genetic laboratory for analysis to check for fetal chromosome abnormalities and provide diagnostic information.
  Non-invasive prenatal testing (NIPT): involves a blood test for pregnant women to screen for chromosomal abnormalities such as Down syndrome and other aneuploidies. This test collects the baby’s DNA from the mother’s blood and can also determine the baby’s gender as early as 10 weeks of pregnancy. NIPT offers a safe and effective method for early detection, providing valuable information about the fetus without the need for invasive procedures like amniocentesis or chorionic villus sampling.
• Pre-conception counselling: is recommended for individuals with a history of pregnancy complications or current health conditions that may impact future pregnancies. Consulting with a fetal maternal medicine expert allows for the development of a proactive plan aimed at improving pregnancy outcomes through effective management measures.
• Genetic testing: offered to patients with a family history of genetic disorders. During this process, we collect a blood sample and isolate your DNA to examine potential changes in chromosomes and genes that may lead to various health conditions and disorders. We offer personalized guidance to help patients better understand their genetic risks and make informed decisions about their health.List of genetic testing:- Chromosomal analysis by next generation sequencing.- Non-invasive prenatal test.- Gene panel testing for different diseases.

  – Targeted mutation screening for known familial mutations.

  – Hereditary cancer panel (ovarian and breast).

  – Whole exome sequencing.

  – Micro-array.