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Prenatal Genetics
Comprehensive prenatal genetic testing and risk assessment to identify inherited and chromosomal conditions early in pregnancy, supporting informed decision-making for expecting parents.
Consultant Clinical Geneticist & Rare Disease Specialist
Dr. Mayuri Yeole
Central India's first DM Medical Geneticist
MBBS, MD (Pediatrics), DM (Medical Genetics)
Clear answers and compassionate guidance for families facing genetic and rare conditions. From accurate diagnosis to simple language counselling, you are supported at every step.
Consultations Mon to Sat, 9:00 AM to 6:00 PM
Care backed by genuine expertise
- Central India's first DM Medical Geneticist
- Gold Medalist, MD Pediatrics (JNMC, Sawangi, Wardha)
- DM Medical Genetics, Kasturba Medical College, Manipal
- Young Researcher Award, Manipal Academy of Higher Education
Welcome to Novagen Genetics Clinic
Genetics, explained with clarity and care
Dr. Mayuri Yeole is a Clinical Geneticist and Pediatrician with a distinguished academic and clinical background. She earned her MD in Pediatrics from JNMC, Sawangi, Wardha, graduating as a Gold Medalist, before specialising in Medical Genetics at Kasturba Medical College, Manipal.
Her expertise spans reproductive genetics, neurodevelopmental and metabolic disorders, skeletal dysplasias, and hematological conditions. She is dedicated to making genetics understandable for families and clinicians alike, because she believes genetics is no longer the medicine of the future, but a vital part of healthcare today.
The clinic
A clinic built around your family
Novagen Genetics Clinic is a dedicated genetics and rare disease centre in Central India.
We bring evaluation, testing, and counselling together in one place, so families do not have to navigate a fragmented system during an already difficult time. Our belief is simple: a genetic diagnosis deserves clear answers and steady support, not just a report.
Hospital Attachments
One place for the whole journey
From the first consultation through testing, results, and next steps, your care stays joined up and personal.
Counselling in plain language
We explain risks, options, and results without jargon, so you can decide with confidence.
Support beyond the diagnosis
For rare diseases, we help you weigh treatment options and navigate government schemes and financial aid.
Testing matched to your needs
We recommend the most appropriate, cost-effective tests, and reanalyse complex cases as the science advances.
When should you see a genetic specialist?
If any of these sound familiar, a genetic evaluation can bring clarity. You do not need a diagnosis to come in; bringing your questions is enough.
An undiagnosed condition
A child or adult with developmental delay, birth differences, or symptoms that have not yet been explained.
A family history
A known or suspected inherited condition, or close relatives with similar or early-onset illness.
Planning a pregnancy
Questions about hereditary risk, consanguinity, or how to prepare before conceiving.
Recurrent pregnancy loss
Repeated miscarriage, or a previous pregnancy affected by a genetic condition.
A complex genetic report
An inconclusive or hard-to-interpret test that needs expert review or reanalysis.
Reassurance and guidance
You simply want to understand your risks and options with someone who explains clearly.
What we do
Services at Novagen Clinic
Our aim is to bring clarity, compassion, and precision to every diagnosis -
helping families make informed decisions and clinicians deliver the best possible care.
Neuromuscular and neurogenetic disorders
Diagnosis and management of genetic conditions affecting the brain, nerves, and muscles, including inherited neuropathies, muscular dystrophies, and neurodevelopmental disorders.
Metabolic disorders
Evaluation and genetic testing for inherited metabolic disorders that affect energy production and metabolism, enabling early diagnosis, treatment planning, and long-term management.
Skeletal dysplasia
Specialized genetic assessment of skeletal dysplasias and growth disorders, focusing on bone development abnormalities, short stature conditions, and related inherited syndromes.
Thalassaemia, haemophilia and other blood disorders
Genetic diagnosis, carrier screening, and counselling for inherited blood disorders such as thalassaemia, haemophilia, and other hematological genetic conditions.
Genetic counselling centre
Personalized genetic counselling services to help individuals and families understand genetic test results, inherited risks, and available testing options with clarity and confidence.
At Novagen Genetics Clinic, we offer comprehensive genetic evaluation, testing, and counselling for individuals and families across all age groups. Our services include prenatal and reproductive genetics, pediatric and adult genetic disorders, metabolic and neurogenetic conditions, skeletal and blood disorders, as well as cancer, diabetes, and obesity genetics. We also specialize in accurate interpretation of genetic reports, reanalysis of complex or inconclusive cases, and personalized guidance for long-term care and family planning.
In the press
Media mentions
Dr. Yeole's work in genetics and rare disease, recognised across leading regional publications.
Your questions, answered
Frequently asked questions
Genetics can feel complex, so we have answered the questions our patients and families ask most.
A Clinical Geneticist is a doctor who specializes in identifying, diagnosing, and managing conditions caused by changes in genes or chromosomes. They help interpret genetic tests, explain results in simple terms, and guide families on treatment options, preventive measures, and future planning.