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Understand your baby's genes for a


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.

Perfectly Safe and Painless

It only requires a tiny drop of cord blood for testing.

Clinically validated technology

It uses high-density single nucleotide polymorphism (SNP) microarray platform for testing, which is the recommended first-tier genetic investigation for many conditions, including autism and intellectual disability.

Internationally certified laboratory

The sample will be tested by our CLIA-certified clinical lab partner based in South Korea. Managed by USFDA, CLIA sets stringent quality standards for labs performing tests on human specimens to ensure accurate, reliable and timely results. Currently, only CLIA-certified labs can report clinical genetic testing results to patients in the United States

Detailed report insights

A detailed interpretation of your baby’s test results will be provided within 6 to 8 weeks after the delivery of your baby. The report will include recommendations to help you make informed choices about your baby’s condition.

Hassle-free Sample Collection

Collection of the test specimen is conducted as a part of the cord blood banking process. Once the quality check of the cord blood for banking is completed, the remaining blood will be processed and send to our clinical laboratory partner for testing

The risk of gene variants or abnormalities

A gene is composed of a group of deoxyribonucleic acid (DNA). Every gene has a complete piece of DNA and has its genetic blueprint. This sequence determines the genetic information of each gene and determines what the parents pass on to their children including physical and psychological characteristics such as the child’s height, memory, appearance, etc. If the sequence of the DNA that makes up a gene is abnormal, the genetic information contained in it will cause genetic diseases due to errors.

Knowledge is power. Early Intervention saves lives.

The early stages of life are the most crucial as they are foundation of a child’s future health and development. While physical disabilities such as visual impairments can be identified before the child turns three, developmental disorders such as autism are not well visible so they are more likely to be diagnosed after the age of three.

Why should you consider Bebegene?

Identify Gene Variants for Disease Prevention

It can also identify potential disease-causing variants related to 6 medical conditions so that you can take steps to delay, manage or even prevent the onset of the condition that your child is predisposed to.

Accurate Detection of Chromosomal Abnormalities

This genetic screening test can accurately identify the early onset of 117 disorders that are associated with symptoms such as autism and ADHD by analyzing more than 250,000 chromosome regions.

Researches have shown

80% of the Autism spectrum disorder (ASD) cases are genetically related. Relatively, 1 in 27 people will be diagnosed with Autism and usually be detected after 3 years of age. The symptoms include poor verbal, abnormal facial and body language and poor social communication. The severity of the disorders depends on the interventions. If the child is carrying disease genes, you may get in time to choose an appropriate intervention plan which can significantly improve child’s cognitive ability.

80% of the ADHD cases are genetically related. On average, 1 in every 14 people is diagnosed with ADHD. The child usually will have symptoms such as poor concentration, impulsive behavior or other illness which could have a significant impact on later life. The severity of the disorders is highly dependent on the time of intervention. Studies have shown that appropriate medication can significantly help some people with ADHD function better. The early detection may facilitate a faster access to intervention.

About 1 in every 10 children under 14 years old may have childhood asthmas. The Hong Kong Asthma Society indicated that majority of the asthma cases are genetically related.The likelihood of getting asthmas or other respiratory conditions such as allergic rhinitis and eczema is higher if the siblings had asthmas-related indications.

The early detection may facilitate a faster access to intervention
which can significantly improve child’s condition.

Conditions caused by Genetic Mutations


Breathing difficulty, wheezing and shortness of breath


Inability to concentrate and hyperactivity


Nose inflammation triggered by allergens


Liver disease, central nervous system disorders or death


Eczema and itching


Partial or complete inability to Hear

The more you know about your baby, the better equipped you can be to address any potential health problems.

Screening your newborn will facilitate early treatment and prevent long term detrimental effects to your baby’s health.

Understand your baby’s gene for a healthier future

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.

Symptoms related to disorders caused by chromosomal abnormalities

Developmental disorders

Include Autism spectrum disorders, Social skill deficit, Learning disability, Intellectual disability.

Internal organ disorders

Include Cardiac anomaly, Kidney dysplasia, Immune deficiency, Dysgenitalism

Physical disability

Include skull deformity, Muscular hypotonia, Growth delay, Visual impairment

Intellectual Disability

Include ADHD, Delusion, Anxiety disorder, Manic-depressive illness

Frequently Asked Questions

Who can sign-up for bebegene®  ?

As the baby’s Cord blood or Buccal Sample is required for testing, expectant mothers can sign-up for bebegene service whether they have signed up for cord blood banking or via Buccal Swab.

Since my baby’s cord blood will be used for testing, will it affect the cord blood unit for future medical use?

bebegene® only requires 0.1ml of residual cord blood for testing. Residual blood is the remaining cord blood after going through the cord blood banking quality control checks. This will not affect the volume and usability of the cord blood unit that you have stored with us.

Since the hospital has already conducted tests on my baby, do I still need bebegene®?

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.

What should I do if the test result is positive?

Genetic counseling service is available upon request. Our qualified genetic counselor will help you understand the result better and provide holistic advice on the follow-up options that you can take.

Disclaimer and Test Limitation

bebegene® genetic screening is tested by Eone-Diagnomics Genome Centre (EDGC), a CLIA-certified clinical lab based in South Korea with leading-edge technology for genome analysis. EDGC has a quality management system in place to ensure maximum accuracy of screening results. The test is only highly accurate for chromosomal abnormalities of aneuploidies, deletions and duplications (>200kb). As with any screening tests, false positive or false negative results cannot be completely eliminated due to various reasons including but not limited to specimen quality and other variables. This is a genetic screening test related to the genetic predisposition developmental disorders. It cannot be considered as a diagnostic test. Hence, the risk of a disorder should never be precluded solely on the basis of screening. If pathogenic variants are detected, follow up testing is recommended to confirm the results. Signs or symptoms observed should be followed up immediately by a professional healthcare provider.


1. Genetic profile and clinical application of chromosomal microarray in children with intellectual disability in Hong Kong. Hong Kong Med J. 2018;24:451-9.