Overview
The Fetal Medicine Team provides a wide range of prenatal screening, diagnostic, therapeutic and counselling services to pregnant women in Hong Kong and overseas as either public and private patients.
Prenatal Screening
- Expanded Carrier Screening (ECS)
- Fragile X-screening
- First trimester Combined Down syndrome screening using Nuchal translucency and biochemical markers (OSCAR)
- First trimester Preeclampsia Screening
- Second trimester biochemical Down Syndrome Screening
- Non-invasive prenatal testing of Down syndrome using circulating cell free fetal DNA (NIPT)
- First trimester fetal morphology scan
- Second trimester Fetal morphological scan
Prenatal Diagnostic procedures
- Chorionic villus sampling
- Amniocentesis
- Cordocentesis
Fetal genetic diagnosis
- Standard Karyotyping
- Rapid testing: PCR, FISH, BoBs Assay
- Comprehensive Fetal DNA Chip (CMA) and next-generation sequencing including whole exome sequencing (WES) and whole genome sequencing (WGS)
Fetal therapy
- Fetoscopic laser photocoagulation for twin-twin transfusion syndrome or other complicated monochorionic twin pregnancies
- Selective fetocide for complicated twin pregnancies
- Intrauterine transfusion (IUT) for fetal anaemia
- Shunting for fetal pleural effusion, macrocystic congenital pulmonary airway malformation (CPAM), lower urinary tract obstruction (LUTO), etc.
- Fetoscopic Endoluminal Tracheal Occlusion (FETO) for congenital diaphragmatic hernia (CDH)
- Other therapies, such as radiofrequency ablation (RFA) for bronchopulmonary sequestration (BPS) and vascular embolization for placental chorioangioma
Genetic Counseling
- Explanation and discussion with parents for abnormal or complicated genetic test results, with guidance on the future investigation and management

