At Sunway Medical Centre, our Genomic Medicine Centre is backed by cutting-edge genomic science, clinical expertise and our internationally accredited laboratories. We translate complex genomic insights into actionable medical decisions β ensuring that every patient receives care uniquely tailored to their genetic profile.
Our services extend beyond genomic testing. We provide comprehensive genetic counselling and a full spectrum of genetic testing services for individuals and families across all life stages.
VIEW OUR SERVICES
Our experienced genetic counsellors provide professional consultation that aims to:
Genetic testing analyses your DNA to:
Our clinical genetic services are designed to support patients who are experiencing unexplained medical conditions, birth defects, or a family history of genetic disorders. We provide comprehensive evaluations, including:
Understanding your genetic risk for cancer is crucial for early detection, prevention, and personalised treatment options. Our cancer genetic counselling services include:
This genetic test identifies inherited mutations associated with an increased risk of various cancers. Early detection of these mutations enables individuals and healthcare providers to take proactive steps in surveillance, prevention, and treatment strategies. This panel analyses multiple genes known to significantly increase the risk for hereditary cancer syndromes.
Genetic counselling before and during pregnancy can provide valuable insights into the health of both mother and baby. Our prenatal genetic counselling services include:
This comprehensive genetic test is designed to identify whether an individual is a carrier of inherited genetic conditions. Carriers typically show no symptoms but can pass these conditions on to their children. This screening assesses the risk of passing on over 400 autosomal recessive and X-linked disorders, regardless of ethnic background.
This test assesses carrier status for more than 400 autosomal recessive and X-linked genetic conditions, including but not limited to:
Expanded newborn screening is a biochemistry test that identifies inherited metabolic disorders that can lead to identifies inherited metabolic disorders that can lead to serious health problems if left untreated. Early detection allows for timely interventions to prevent irreversible damage, developmental delay, or even death. This test screens for a broad range of metabolic conditions using advanced analytical techniques.
This test covers 30++ inherited metabolic disorders conditions across multiple categories, including:
Our team consists of experienced clinical geneticists, genetic counsellors, and multidisciplinary specialty consultants.
We focus on individualised care and ensuring that patients and families are well-informed and supported throughout their genetic healthcare journey.
We collaborate with accredited local and international laboratories to ensure the quality of testing and interpretation of results.
From diagnosis and counselling to treatment and long-term follow-up, we are here to guide you every step of the way.
This will be provided by our experienced genetic counsellors.
You may be referred by your doctor or contact us directly to arrange an appointment.
We discuss your concerns, family history, testing options and possible outcomes.
A sample (blood, saliva, or tissue) is collected for analysis.
Results are reviewed and explained, including implications and management plan for you and your family.
Genetic Counsellor
Genetic Counsellor
Visiting Genetic Counsellor
If youβre interested in learning more about our genomic medicine services or would like to schedule a consultation, please feel free to contact us.
