Our Services
Patients receive comprehensive care from expert medical teams that focus not only on specific diseases and disorders,
but also on caring for the whole person
Ultrasound
Ultrasound, also known as sonography, is a non-invasive medical imaging technique that uses high-frequency sound waves to create real-time images of structures within the body.
Fetal Invasive Procedure
Fetal invasive procedures are medical interventions that involve accessing the developing fetus inside the uterus for diagnostic or therapeutic purposes.
Genetic Services
Genetic services in fetal medicine involve the use of genetic testing and counseling to assess the genetic health of a developing fetus during pregnancy.. These services play a crucial role in identifying
NT Scan
"NT scan," refers to a Nuchal Translucency (NT) scan.It is a prenatal screening test that assesses the risk of chromosomal abnormalities, particularly Down syndrome and other genetic conditions
- Purpose
- Timing
- Procedure
- Risk Assessment
- Follow-Up Testing
Anomaly Scan
An Anomaly Scan, also known as a Level 2 ultrasound or a fetal anatomy scan , is a detailed ultrasound examination performed during pregnancy to assess the development and structure of the fetus.
- Detection of Abnormalities
- Follow-Up Actions
- Procedure
- Preparation
- Timing
Fetal 2D Echo
A Fetal 2D Echocardiogram (echo) is a specialized ultrasound examination that focuses specifically on the heart of the developing fetus. It is used to assess the structure and function of the fetal heart.
- Purpose
- Procedure
- Detection of Cardiac Abnormalities
- Follow-Up and Management
- Importance
Amniocentesis
Amniocentesis is a prenatal diagnostic procedure that involves extracting a small amount of amniotic fluid from the amniotic sac surrounding the developing fetus that provide information the development
- Timing
- Procedure
- Risks and Considerations
- Decision and Counseling
- Purpose
Cordocentesis
It is also known as percutaneous umbilical blood sampling or fetal blood sampling,is a prenatal diagnostic procedure that involves extracting a small sample of blood from the fetal umbilical cord
- Indications
- Timing
- Miscarriage Risk
- Bleeding and Hematoma
- Infection
Chorionic Villus Sampling
Chorionic Villus Sampling (CVS) is a prenatal diagnostic procedure that involves collecting a small sample of tissue from the placenta, specifically from the chorionic villi.
- Ultrasound Guidance
- Needle Insertion
- Blood Sample Collection
- Risks and Considerations
Multivessel Doppler
Multivessel Doppler is a medical imaging technique that uses Doppler ultrasound technology to assess blood flow in multiple blood vessels within the body. It helps healthcare providers decisions patient care
- Ultrasound Probe
- Color Doppler
- Spectral Doppler
- Obstetrics
- Cardiology
3D/4D
3D and 4D ultrasound are advanced imaging techniques use sound waves to create three-dimensional(3D) images or moving real-time 3D images(4D) of the developing baby
- Purpose
- Procedure
- Detection of Cardiac Abnormalities
- Follow-Up and Management
- Importance
Neurosonogram
A neurosonogram, also known as a neonatal neurosonogram or neonatal cranial ultrasound, is a specialized ultrasound examination that focuses on imaging the brain structures of newborns
- Ultrasound Probe
- Imaging
- Evaluation
- Follow-Up and Monitoring
- Consultation
Fetal Blood Transfusion
Fetal blood transfusion, also known as intrauterine transfusion (IUT), is a medical procedure performed during pregnancy to treat certain conditions in which the fetus has blood
- Infection
- Preterm Labor
- Fetal Injury
- Maternal Complications
- Transfusion
Karyotype
A karyotype is a laboratory test that analyzes the chromosomes in a person's cells are structures within cells that contain the genetic information in the form of DNA ordered by size and shape
- Cell Collection
- Cell Culturing
- Chromosome Staining
- Microscopic Analysis
- Photographs
Down Syndrome
Down syndrome,also known as Trisomy 21,is a genetic disorder caused by the presence of an extra copy of chromosome 21.It is one of the most common genetic conditions
- Facial Features
- Low Muscle Tone
- Cognitive Delays
- Heart Defects
- Gastrointestinal Issues