CENTRE for PRECISION HEALTH & PAEDIATRICS

Personalized Care for Every Generation

🎉 Clinic Opening in May 2026

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Our Services

Comprehensive precision medicine and pediatric care tailored to each child's unique genetic profile

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Genomic Medicine

Advanced genetic testing and analysis using state-of-the-art sequencing technologies to identify genetic variations and provide personalized treatment strategies.

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Precision Diagnostics

Cutting-edge diagnostic services combining clinical expertise with molecular insights to accurately diagnose complex pediatric conditions.

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Rare Disease Diagnosis

Expert evaluation and diagnosis of rare and undiagnosed diseases through comprehensive genetic and clinical assessment.

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Personalized Treatment

Tailored therapeutic approaches based on individual genetic profiles, ensuring optimal treatment efficacy and safety.

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Family Counseling

Compassionate genetic counseling to help families understand genetic conditions, inheritance patterns, and reproductive options.

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General Paediatrics and Newborn Care

Comprehensive pediatric care from birth through adolescence, including routine check-ups, vaccinations, developmental monitoring, and acute illness management.

About Our Centre

Pioneering precision medicine for the next generation

Excellence in Precision Pediatrics

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.

  • Board-certified clinical geneticist
  • Access to state-of-the-art genomic sequencing facilities
  • Multidisciplinary care coordination
  • Evidence-based clinical practice
  • Family-centered approach

Our Mission

We are committed to transforming pediatric healthcare through precision medicine, providing accurate diagnoses and personalized treatments that improve outcomes for children with genetic conditions.

Our Vision

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.

Our Values

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.

About Dr Saumya Jamuar

Board-Certified Clinical Geneticist & Senior Consultant

Dr Saumya Jamuar

Dr Saumya Jamuar

MBBS, MRCPCH (UK), FAMS, FACMG

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.

Notable Achievements

  • Identified the world's first known case of a rare genetic syndrome named "Jamuar Syndrome"
  • Published research in top-tier journals including The New England Journal of Medicine, Nature Genetics, Neuron, and Nature Communications
  • Leading expert in childhood undiagnosed diseases and precision medicine
  • Extensive experience in genomic medicine and clinical genetics

Dr Jamuar in the News

Featured articles and media coverage on precision medicine and rare disease research

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HealthXchange / KKH
September 2020

KKH and A*STAR identify world's first known case of Jamuar Syndrome

Discovery of a rare genetic syndrome named after Dr Jamuar, published in Nature Communications.

Read Article →
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National Precision Medicine Programme
Featured Article

No Child's Play In Paediatric Precision Medicine

Dr Jamuar discusses the role of precision medicine in diagnosing rare genetic diseases in children.

Read Article →
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The Straits Times
September 2024

Gene detectives: KKH diagnostic programme uncovers rare disorders, helps over 300 families find answers

Dr Jamuar and the BRIDGES programme help families with children afflicted by rare genetic disorders find answers through advanced genomic testing.

Read Article →
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CBmE Podcast
Podcast Interview

Precision Medicine with Saumya Shekhar Jamuar

Discussing precision medicine, genomics data sharing, and carrier screening in family planning.

Listen →
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PRECISE IHCC Conference 2024
Conference Video

Speaker at PRECISE IHCC Conference 2024 on Rare Genetic Diseases in Singapore

Dr Jamuar presents on rare genetic diseases and precision medicine initiatives in Singapore at the international conference.

Watch Video →
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The UGDH Foundation
Organization

Scientific Advisor - UGDH Foundation

Supporting research and families affected by Jamuar Syndrome (DEE84) worldwide.

Learn More →

Get in Touch

Clinic opening in May 2026 - We're here to answer your questions and schedule consultations

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Phone

+65 6452 5288

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Email

enquiries@drjamuar.com

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Location

3 Mount Elizabeth
#10-06
Mount Elizabeth Medical Centre
Singapore 228510

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Hours

Mon-Fri: 9AM to 5PM
Sat: 9AM to 1PM