bebegene® Newborn Genetic Screening
Screens 0-3 years babies with more than 120 conditions caused by chromosomal abnormalities and disease-causing gene variants, providing you an expanded insight of your baby’s health condition.
Screens 0-3 years babies with more than 120 conditions caused by chromosomal abnormalities and disease-causing gene variants, providing you an expanded insight of your baby’s health condition.
Sample collection is as simple and seamless as it can be done during the time of birth delivery. Only a small fraction of the cord blood would be collected for screening.
Identify more than 120 conditions caused by chromosomal abnormalities and disease-causing gene variants, providing you an expanded insights of your baby’s health condition.
Your baby’s sample will be analysed using SNP chromosomal microarray technology, which is the recommended first-tier genetic test for conditions, such as autism and intellectual disability.
The test is performed by a recognized clinical laboratory partner in South Korea. The laboratory is also equipped with CAP and CLIA accreditation for its technology and excellence for other line of services including Microarray technology and Direct-to-Consumer genetic testing (DTC).
A detailed interpretation of your baby’s test results will be provided one month after the delivery of your baby. The report will include recommendations to help you make informed choices about your baby’s condition.
Screening your newborn will facilitate early treatment and prevent long term detrimental effects to your baby’s health.
Expectant mothers can sign up bebegene® service prior birth delievery. This service must be prescribed by doctor who will explain the
details about the test to ensure the test is suitable for your baby. Do enquire us now for more details.
Sample collection is as simple and seamless as it can be done during the time of birth delivery. Only a small fraction of the cord blood would be collected for screening.
Bebegene® provides you an expanded coverage of conditions beyond the checks conducted at the hospital. With the access to more information of your baby’s health, you can take preemptive measures to manage the potential conditions that your child is predisposed to. This small step can help to make a difference in your child’s development and overall health.
Genetic counselling service is available upon request. Our qualified genetic counsellor will help you understand the result better and provide holistic advice on the follow-up options that you can take.
SBT/PM-042/Rev.00