Early detection for effective disease management. Your first step to a healthy life.
Explore our Services
An accurate and affordable
pre-pregnancy and pregnancy screening test for 155 genetic disorders.
Endometrial Receptivity Test
MIRA miRNA-based Receptivity Analysis helps to identify your best time for embryo transfer more reliably.
Preimplantation Genetic Screening
Cordlife PGS (Preimplantation Genetic Screening) is the procedure of evaluating embryos for chromosomal aneuploidy, the presence of either addition or loss of chromosomes in embryos generated from chromosomally normal parents
Non-Invasive Prenatal Testing (NIPT)
From a simple blood draw as early as 10 weeks into your pregnancy, NIPT services screens for the most common chromosomal abnormalities that can affect your developing baby’s future.
NEWBORNS & CHILDREN
bebegene® Genetic Screening
Newborn genetic screening can help to detect chromosomal abnormalities as well as the presence of risk factors early so that you are better equipped to address any potential problems to avoid the development of serious symptoms that may go undetected as the baby grows up
Most comprehensive newborn metabolic screening for 0-6 months.* Screening your newborn will facilitate early treatment and prevent long term detrimental effects to your baby’s health.
NEWBORNS & CHILDREN
Cordlife Talent DNA Testing
Every child is unique. Cordlife TALENT is a DNA testing service that uses cutting-edge technology to help you learn more about your child. Our insight reports will include information about your child in the key categories:
Lifestyle Genetic Test
Each of us has a unique set of inherited genes that gives us a different makeup. With the personalised insights provided by our detailed tests’ reports, you can find out how your gene expressions affect your physiological behaviour, abilities, and more to optimise your overall well-being.
Early Detection for Effective Disease Management.
Your First Step to a Healthy Life.
Did You Know?
Screening for your newborn will facilitate early detection and treatment with the hopes of preventing and managing possible long-term effects on your baby’s health.
About 1 in every 1682 babies is expected to be born with an inherited metabolic disorder, which may cause developmental issues and lifelong complications such as mental retardation, physical disability and in some instances, death, if it is left untreated.1
About 1 in every 10 children may have asthmas.The chances of getting asthmas is higher if the siblings had asthmas-related indications.2
Autism spectrum disorder (ASD) cases are genetically related. The early detection may facilitate a faster access to intervention which can significantly improve child’s cognitive ability. 3
One in every 20 children may be suffering from hyperactivity, resulting in poor concentration, impulsive behavior or other illness which could have a significant impact on later life. 4
1Evaluation of the 18-month "Pilot Study of Newborn Screening for Inborn Errors of Metabolism" in Hong Kong. HK J Paediatric (New Series) 2020;25:16-22
2Childhood asthmas are genetically related. Hong Kong Asthma Society website. https://www.hkasthma.org.hk/hk/press-releases/926. Accessed June 18, 2020.
3Autism risk from inherited genes. Autism Speaks website. https://www.autismspeaks.org/. Accessed on February 20, 2023.
4General Prevalence of ADHD. Children and Adults with Attention-Deficit/Hyperactivity Disorder (CHADD) Organisation website. https://chadd.org/about-adhd/general-prevalence/. Accessed on February 20, 2023.