Personalized Care for Every Generation
🎉 Clinic Opening in May 2026
Get in TouchComprehensive precision medicine and pediatric care tailored to each child's unique genetic profile
Advanced genetic testing and analysis using state-of-the-art sequencing technologies to identify genetic variations and provide personalized treatment strategies.
Cutting-edge diagnostic services combining clinical expertise with molecular insights to accurately diagnose complex pediatric conditions.
Expert evaluation and diagnosis of rare and undiagnosed diseases through comprehensive genetic and clinical assessment.
Tailored therapeutic approaches based on individual genetic profiles, ensuring optimal treatment efficacy and safety.
Compassionate genetic counseling to help families understand genetic conditions, inheritance patterns, and reproductive options.
Comprehensive pediatric care from birth through adolescence, including routine check-ups, vaccinations, developmental monitoring, and acute illness management.
Pioneering precision medicine for the next generation
The Centre for Precision Health and Paediatrics represents a new paradigm in children's healthcare, combining advanced genomic technologies with comprehensive pediatric expertise.
Our multidisciplinary team brings together specialists in clinical genetics, genomic medicine, pediatrics, and genetic counseling to provide holistic, evidence-based care.
We are committed to transforming pediatric healthcare through precision medicine, providing accurate diagnoses and personalized treatments that improve outcomes for children with genetic conditions.
To be the leading center for precision pediatric medicine, where every child receives care tailored to their unique genetic makeup, and families find answers, hope, and expert support.
Excellence, compassion, innovation, and family partnership guide everything we do. We believe in treating each child as an individual and supporting families throughout their healthcare journey.
Board-Certified Clinical Geneticist & Senior Consultant
Dr Saumya Jamuar is a Board Certified Clinical Geneticist and brings extensive expertise in genomic medicine, pediatric genetics, and rare disease diagnosis to the Centre for Precision Health and Paediatrics.
Dr Jamuar was previously a Senior Consultant at KK Women's and Children's Hospital in Singapore. He held several prestigious leadership positions including Director of the SingHealth Duke-NUS Institute of Precision Medicine, Inaugural Head of SingHealth Duke-NUS Genomic Medicine Center, Lead Principal Investigator of the Singapore Childhood Undiagnosed Disease Programme, and is the Chair of Chapter of Genomic Medicine, Academy of Medicine, Singapore.
His academic journey includes graduation from the National University of Singapore, pediatric training at SingHealth, and fellowship training in clinical genetics at Harvard Medical School. He also completed a post-doctoral fellowship in the Christopher A. Walsh Lab at Harvard Medical School.
Featured articles and media coverage on precision medicine and rare disease research
Discovery of a rare genetic syndrome named after Dr Jamuar, published in Nature Communications.
Read Article →Dr Jamuar discusses the role of precision medicine in diagnosing rare genetic diseases in children.
Read Article →Dr Jamuar and the BRIDGES programme help families with children afflicted by rare genetic disorders find answers through advanced genomic testing.
Read Article →Discussing precision medicine, genomics data sharing, and carrier screening in family planning.
Listen →Dr Jamuar presents on rare genetic diseases and precision medicine initiatives in Singapore at the international conference.
Watch Video →Supporting research and families affected by Jamuar Syndrome (DEE84) worldwide.
Learn More →Clinic opening in May 2026 - We're here to answer your questions and schedule consultations
+65 6452 5288
3 Mount Elizabeth
#10-06
Mount Elizabeth Medical Centre
Singapore 228510
Mon-Fri: 9AM to 5PM
Sat: 9AM to 1PM