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Dr Koh Ai Ling

Dr Koh Ai Ling

MB ChB (Edinburgh, UK), MRCPCH (RCPCH, UK), M Med (Paed) (Spore)

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

Clinical Lead, Paediatrics SingHealth Duke-NUS Genomic Medicine Centre
Therapeutics Lead SingHealth Duke-NUS Genomic Medicine Centre
Consultant Genetics Service KK Women's and Children's Hospital

Profile

Education

MB ChB (U of Edinburgh, United Kingdom) 2009
MRCPCH (RCPCH, United Kingdom) 2016
M Med (Paed) (NUS, Singapore) 2016

Professional Appointments and Committee Memberships

Awards

Research Interests

Publications

Koh AL, Tan ES, Brett MS, Lai AH, Jamuar SS, Ng I, Tan EC. The spectrum of genetic variants and phenotypic features of Southeast Asian patients with Noonan syndrome. Molecular genetics & genomic medicine. 2019 Feb 19:e581.
B McNeills, R James, AL Koh, T Sparkes, S Shantikumar. (2011). Get Ahead! Medicine: 300 SBAs for Finals. Hodder Education, London, UK

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