Some health conditions run in families. Others happen due to changes in genes that we may not even know about. Understanding these changes can help with early diagnosis, better management, and informed family planning. At Manipal Hospitals, Kanakapura Road, Genetics Department offers comprehensive clinical evaluation, advanced molecular diagnostics, and family-focused counselling for adults, children, and expectant parents.
At Manipal Hospitals, Kanakapura Road, advanced laboratory science meets experienced clinical genetics and compassionate counselling—so families don’t just receive reports, they gain real understanding and clear next steps.
The genetics team includes clinical geneticists, genetic counsellors, molecular technologists, and bioinformaticians who work hand in hand with specialists in obstetrics, paediatrics, oncology, cardiology and other departments. This close collaboration ensures that every test result is carefully interpreted and meaningfully applied to patient care.
Families trust us because we offer:
Accredited molecular and cytogenetic laboratories for rapid, reliable testing and interpretation
Multidisciplinary team offering clinical genomics, counselling, and long-term follow-up
Seamless integration with prenatal care, newborn screening, and oncology services for actionable results
Clear, family-centred communication and stepwise guidance through testing choices and outcomes
Knowing whether a genetic condition runs in a family can help couples plan their future with informed decisions. Carrier testing helps identify people who carry an underlying genetic change that usually does not affect their own health but could be passed on to children. At Manipal Hospital Kanakapura Road, carrier testing is offered with clear explanations,…
The Genetics Department at Manipal Hospital Kanakapura Road brings diagnostics, counselling, and clinical care together under one roof. Care is tailored to the clinical history, family context, and reproductive goals. The centre focuses on early detection, evidence-based interpretation, and ongoing follow-up to reduce uncertainty and improve health across generations. Collaborative referral pathways and streamlined sample logistics support timely decision-making with surgical, medical, and allied teams.
We help families understand risks, make informed decisions, and plan future care with confidence.
We provide:
Genetic counselling for inherited conditions and pregnancy planning
Chromosome testing (karyotype, microarray, FISH)
Prenatal testing (CVS, amniocentesis)
Non-invasive prenatal screening (NIPT)
Newborn screening for metabolic disorders
Biochemical Screening in Pregnancy-Double/Quad study, Pre-eclampsia screening
Testing for single-gene conditions such as thalassemia, SMA, Duchenne muscular dystrophy
Advanced sequencing tests (whole exome, gene panels)
Hereditary cancer testing including BRCA
Patients visit the Genetics department at Manipal Hospitals Kanakapura Road for expert diagnosis, advanced treatment, and personalized care. The department specializes in managing Carrier testing, ensuring world-class medical support for patients.
The Genetics department at Manipal Hospitals Kanakapura Road provides a wide range of treatments, including:
To book an appointment with a Genetics expert at Manipal Hospitals Kanakapura Road, please call 1800 102 5555. Our dedicated team will assist you in scheduling a convenient consultation.
The Genetics department is led by highly qualified specialists, including:
For your initial consultation at Manipal Hospitals Kanakapura Road, please bring:
Providing these documents will help our specialists ensure a comprehensive diagnosis and personalized treatment plan.
Manipal Hospitals Kanakapura Road is a preferred choice for Genetics due to:
We are committed to providing world-class healthcare with compassionate service.
At Manipal Hospitals Kanakapura Road, we offer facilities such as:
We provide:
Genetic counselling for inherited conditions and pregnancy planning
Chromosome testing (karyotype, microarray, FISH)
Prenatal testing (CVS, amniocentesis)
Non-invasive prenatal screening (NIPT)
Newborn screening for metabolic disorders
Biochemical Screening in Pregnancy-Double/Quad study, Pre-eclampsia screening
Testing for single-gene conditions such as thalassemia, SMA, Duchenne muscular dystrophy
Advanced sequencing tests (whole exome, gene panels)
Hereditary cancer testing including BRCA
Our team ensures precise diagnosis and treatment planning for each patient.
At Manipal Hospitals, Kanakapura Road, advanced laboratory science meets experienced clinical genetics and compassionate counselling—so families don’t just receive reports, they gain real understanding and clear next steps.
The genetics team includes clinical geneticists, genetic counsellors, molecular technologists, and bioinformaticians who work hand in hand with specialists in obstetrics, paediatrics, oncology, cardiology and other departments. This close collaboration ensures that every test result is carefully interpreted and meaningfully applied to patient care.
Families trust us because we offer:
Accredited molecular and cytogenetic laboratories for rapid, reliable testing and interpretation
Multidisciplinary team offering clinical genomics, counselling, and long-term follow-up
Seamless integration with prenatal care, newborn screening, and oncology services for actionable results
Clear, family-centred communication and stepwise guidance through testing choices and outcomes
Normally, genetic testing is done for expected newborns in their fetal stage, or when a hereditary disorder is suspected in a patient. In the first visit, genetic screening is done to evaluate the chances of a hereditary disorder being present.
The department evaluates congenital anomalies, intellectual disability, hereditary cancer syndromes, cardiomyopathies, metabolic disorders, and reproductive risks. Testing is selected to answer the clinical question and often combines molecular, chromosomal, and counselling inputs to reach a clear diagnosis.
Anyone can seek genetic counselling:
Couples planning pregnancy
Pregnant women
Parents of children with health or developmental concerns
Adults with family history of cancer or heart disease
Individuals from consanguineous (close-relative) marriages
Families with autism or unexplained medical conditions
You do not need a confirmed diagnosis to seek counselling. Genetic counselling helps you understand risks and testing options in a clear and supportive way.
Prenatal testing ranges from non-invasive screening using maternal blood to diagnostic procedures such as chorionic villus sampling and amniocentesis. Counselling before and after testing explains benefits, limitations, and likely next steps so parents can make informed decisions.
Genetic counselling helps estimate risks and explain possibilities. It may not always give definite answers, but it helps families make informed decisions with clarity and confidence.
Newborn screening looks for treatable metabolic and endocrine conditions soon after birth. Early detection enables timely treatment that can prevent disability. The centre follows quality assurance practices to ensure accurate and actionable results.
Sometimes ultrasound scans may show soft markers or structural differences. This does not always mean there is a serious problem.
A genetic consultation helps:
Understand what the finding means
Decide if further testing is needed
Discuss possible outcomes
Plan next steps calmly and clearly
Pharmacogenetic testing reveals how genes affect medication metabolism and response. Results guide drug selection and dosing to reduce adverse reactions and improve effectiveness, particularly in oncology, psychiatry, and cardiology.
There are two main types:
Non-invasive tests (NIPT): Blood test from the mother, safe for the baby.
Diagnostic tests (CVS / Amniocentesis): These provide confirmed results and are done under expert supervision.
Before any test, detailed counselling is provided to explain benefits and risks.
Genetic disorders are known to lie dormant among many individuals. This means that they carry the abnormal gene, but it is not active in the person. The abnormal genes can present itself in the next generation, which is why carrier genetic testing is an important step to take before conception.
Genetic counselling is recommended when there is a family history of inherited conditions, recurrent pregnancy loss, unexplained developmental delay, or before and after genetic testing. Sessions cover history, inheritance patterns, testing choices, and practical support delivered with empathy and clear guidance.
Pregnancy at 35 years or above is called advanced maternal age.
It may slightly increase the chance of certain chromosomal conditions, but many women have healthy pregnancies. Screening and proper monitoring help reduce uncertainty.
Consanguinity means marriage between close relatives (for example, cousins).
Such marriages may increase the chance of certain inherited conditions, especially recessive disorders. Genetic counselling can help assess risks and guide testing before or during pregnancy.
Autism can sometimes have a genetic basis. If there is autism, intellectual disability, or developmental delay in the family, genetic evaluation may help:
Understand possible causes
Estimate recurrence risk
Guide future pregnancy planning
If multiple family members have cancer, especially at a young age, genetic testing may help assess hereditary risk.
This can guide:
Early screening
Preventive measures
Testing for other family members
If a specific genetic condition or hereditary cancer syndrome has already been diagnosed in your family, genetic counselling becomes especially important. It can help you:
Understand who in the family may be at risk
Decide who should consider testing
Plan screening or preventive care early
Make informed decisions about pregnancy or family planning
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