Individuals & Families
What is a genetic test?
It is a type of medical test that identifies abnormalities in a person's DNA. Our DNA provides the blueprint for how our bodies grow and develop. Genetic testing is used to find DNA anomalies associated with specific medical conditions and can help determine whether a person has a genetic disease, whether it has been inherited, and the chances of future children or other family members having the same condition.
What is a microarray-based genetic test?
A microarray test can detect stretches of our individual DNA that are either deleted or duplicated. These changes can sometimes result in disease.This test is extremely sensitive and offers, for the first time, an in-depth and comprehensive look into the detailed genetic make-up of an individual.
How is the Sengenics Test different or better than other microarray tests?
The Sengenics Test analyses the entire genome and screens over 400 known genetic syndromes. It is the only array test that uses pre-optimised probes to ensure highly accurate diagnosis. It is certified and endorsed by The International Standards for Cytogenomic Arrays (ISCA). As the cutting-edge, best-of-its-kind microarray genetic test, it has recently been recognised as the ideal tool to be used as the first line of diagnosis by 27 leading medical institutions including Harvard Medical School and the world famous Mayo Clinic.
Who should consider this kind of genetic testing?
You should consider the Sengenics Test if the following situations are relevant to you:-
- You have a child with learning difficulties, delayed development or other noticeable symptoms that your doctor suspects may be a genetic condition.
- Your doctor thinks you may have a genetic disorder and wishes to have an accurate confirmation of the diagnosis before you plan a family.
- You have had recurrent miscarriages or stillbirths, or are planning an advanced age pregnancy. All these situations may suggest an increased risk that your baby could be born with a genetic disorder.
- There is a history of a serious genetic condition that runs in your family.
What are the benefits of the Sengenics Test?
The Sengenics Test will be able to tell you about your or your child's genetic makeup with accuracy and certainty. For most people the relief from uncertainty is extremely important whether the test is positive or negative. If the test is negative, it can mean peace of mind knowing that you or your child are free from major genetic disorders. If the test is positive, you now have advance knowledge so that the appropriate treatment can be given or the condition managed from an early stage. For example, if your test reveals an increased risk of developing a condition later in life, such as diabetes or certain heart disorders, the knowledge can guide you in making better dietary and lifestyle choices for optimum health management. Or, if the test reveals the presence of Autism, early intervention and management can significantly reduce challenges associated with this condition, lessen disruptive behaviour and provide some degree of independence.
Results of the test can also provide useful information when planning for future children.
What support is available if my test is positive?
Sengenics' mission is to go Beyond the Diagnostics. Rather than provide just the test, Sengenics will allow you and your doctor access to its local and international panel of scientists and genetic counselors for advice on potential treatment and/or education programmes to intervene, manage and treat any potential disorders that are identified. This will ensure the best possible support and peace of mind for you.
What type of sample is needed?
Our preferred sample type is whole blood but other types of samples can also be used such as saliva. Your doctor will determine which type of sample to submit for analysis.
When should I expect results, and who will contact me to discuss it?
You should receive a full diagnosis report from your doctor within three (3) weeks from the day the sample is received. This will depend on the individual's particular condition and the locality where the sample was collected from. All patients will have access to Sengenics' recommended Panel of Genetic Counsellors should results be positive in terms of detecting a genetic disorder or condition.
How much does this test cost?
Please refer to the Sengenics Test Fees. 6 or 12-month installment payments with 0% interest are available with selected credit cards from participating banks.
Who should I contact if I have additional questions?
Please contact either one of Sengenics' recommended Panel of Doctors or email your questions direct to enquiries@sengenics.com.
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- LEARNING & BEHAVIOURAL
(HU-LB1)
Specific learning disorders, Autism and neurodegenerative disorders. See detailed syndrome list for full details.
- PHYSICAL (HU-PH1)
Skeletal and dysmorphism disorders. See detailed syndrome list for full details.
- METABOLIC & ORGAN (HU-MO1)
Diabetes, pancreatic, hormonal, eye, kidney, hearing, cardiac, and infertility disorders. See detailed syndrome list for full details.
- HEREDITARY CANCERS (HU-HC1)
A broad range of hereditary cancers. See detailed syndrome list for full details.
- WHOLE GENOME (HU-WG1)

All the above disorders and syndromes. See detailed syndrome list for full details.