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Dr

Dr

MBBS, MRCPCH (UK)

Senior Consultant

KK Women's and Children's Hospital

Specialty: Paediatric Genetics

Conditions Treated by this Doctor:
22q11.2 Deletion Syndrome, Achondroplasia, Citrin Deficiency, Inherited Retinal Diseases, Klinefelter Syndrome, Medium-Chain Acyl-CoA Dehydrogenase Deficiency, Mitochondrial Diseases, Triple X Syndrome, Turner Syndrome.

Clinical Appointments

Deputy Director (Clinical) SingHealth Duke-NUS Institute of Precision Medicine
Senior Consultant Genetics Service KK Women's and Children's Hospital

Profile

Education

Professional Appointments and Committee Memberships

Awards

Research Interests

Genetic disorders
Precision medicine
Neurodevelopmental genetics

Publications

Research Trials

Tags: Paediatric Genetics, 22q11.2 Deletion Syndrome, Achondroplasia, Citrin Deficiency, Inherited Retinal Diseases, Klinefelter Syndrome, Medium-Chain Acyl-CoA Dehydrogenase Deficiency, Mitochondrial Diseases, Triple X Syndrome, Turner Syndrome