The NUWoC Genetics and Genomics programme aims to enhance and expand access to high-quality genetic services throughout the pre-conception, pregnancy, and postnatal journey. We specialise in genetic evaluation, genetic testing, and treatment options while providing support for parents facing difficult decisions.
Our team comprises doctors from the Department of Paediatrics, KTP-NUCMI and Department of Obstetrics & Gynaecology.
Led by: Dr Chin Hui-Lin, Dr Karen Lim
The NUWoC Fetal Medicine Clinic provides specialised care for couples whose baby has been diagnosed with an abnormality, couples who face difficult decisions about their pregnancy due to medical reasons, or couples who require specialised genetic counselling due to risk of a genetic disorder.
For more information, click here.
The NUHS Genomic Assessment Centre (GAC) aligns with the Ministry of Health’s strategy to enhance preventive care for individuals and their family through personalised medicine. At the GAC, patients can:
Read: Genomic Assessment Centre
As part of the national Familial Hypercholesterolaemia (FH) genetic testing programme, NUHS will be launching a FH genetic testing service.
Our genetic counsellors will help individuals and their family members identify FH early and work with them to reduce their risk of premature heart disease.
What is FH?
FH is a condition that affects the body’s ability to process cholesterol. Individuals with FH face a significantly higher risk of experiencing heart attacks at a younger age compared to the general population. It is also a hereditary condition, meaning it can be passed down in families.
Read: What is Familial Hypercholesterolaemia?
The FH genetic testing service at NUHS will be launched in Q4 2025/Q1 2026.
For enquiries about FH genetic testing or GAC at NUHS, please email [email protected].
Complementing these developments, the Division of Paediatric Genetics and Metabolism, Department of Paediatrics at the Khoo Teck Puat – National University Children's Medical Institute, NUH provides specialised services for diagnosis and treatment for both adults and children with confirmed or potential genetic disorders. Learn more about our services here.
