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A/Prof Stacey Tay Kiat Hong

Photo of A/Prof Stacey Tay Kiat Hong
Credential:
MBBS (S'pore), MMed (Paeds) (S'pore), MRCP (Paeds) (UK), MRCPCH (UK)
Designation:
Senior Consultant, Division of Paediatric Neurology, Department of Paediatrics, Khoo Teck Puat - National University Children's Medical Institute, National University Hospital
Senior Consultant, Division of Paediatric Genetics & Metabolism, Department of Paediatrics, Khoo Teck Puat - National University Children's Medical Institute, National University Hospital
Associate Professor, Department of Paediatrics, Yong Loo Lin School of Medicine, National University of Singapore (Research Specialty: Human Genetics)
Specialty:
Paediatrics
Sub Specialty:
Paediatric Genetics and Metabolism, Paediatric Neurology
Medical and Surgical Conditions:
Atrial Septal Defect (Children), Autism (Children), Brain Injury (Newborn), Congenital Heart Conditions (Newborn), Disorders of Sex Development (Children), Epilepsy (Children), Febrile Seizure (Children), G6PD Deficiency (Children), Growth Disorders in Children, Haemophilia (Children), Handwriting Difficulty (Children), Headaches (Children), Hearing Loss (Children), Inborn Errors of Metabolism, Intraventricular Haemorrhage (Children), Marfan Syndrome (Children), Meningitis (Children), Neuromuscular Disorders - Nerve and Muscle Disorders (Children), Paediatric Cataracts, Turner Syndrome (Children), Universal Hearing Screening Programme
Institution:
National University Hospital
National University Health System
Associate Professor Stacey Tay is currently Senior Consultant in the Division of Paediatric Neurology and in the Division of Paediatric Genetics and Metabolism at the Khoo Teck Puat-National University Children's Medical Institute, National University Hospital, as well as Associate Professor of Paediatrics, Yong Loo Lin School of Medicine.

She obtained her basic MBBS medical degree from the National University of Singapore with honours in 1994 and subsequently attained her postgraduate paediatric degrees (MMed, S'pore, MRCP, UK and MRCPCH, UK) in 1997. She won the NUH Young Doctor's Award in 2001 for her research on diagnostic methods in Duchenne Muscular Dystrophy. She became a Fellow of the Academy of Medicine, Singapore in 2004.
 
Her specialist Paediatric Neurology Training was undertaken at the Neurological Institute of New York at Columbia University where she was on a clinical and research fellowship from 2002 to 2004. She pursued her interest in neurogenetic and mitochondrial disorders under the mentorship of Professor Marc C Patterson and Prof Salvatore DiMauro.

Following training, she returned to National University Hospital where she has established the Neurogenetic Clinic, as well as the research and teaching arms of the division, founding a group that studies the genetics of paediatric neurological diseases, and conducts regular paediatric neurology teaching rounds. In her clinical work, she looks after children with neurogenetic disorders, neuromuscular disorders, movement disorders and epilepsy.

A/Prof Tay is actively involved in the special needs community and has professionally supported organisations such as the Muscular Dystrophy Association of Singapore and Ronald McDonald House Charities.

Awards and Honours

NUH Young Doctor's Award, 2001​

Professional Memberships

Fellow of the Academy of Medicine, Singapore​

Research and Publications

  1. Tay SK, Garone C, DiMauro S (2016). Mitochondrial Encephalopathies. International Neurology 2nd Ed.
  2. Aishworiya R, Chan PF, Kiing JS, Chong SC, Tay SK (2016). Sleep Patterns and Dysfunctions in Children with Learning Problems. Annals of the Academy of Medicine, Singapore, 45(11):507-512.
  3. Utami KH, Winata CL, Hillmer AM, Aksoy I, Long HT, Tay SK, . . . Cacheux V (2014). Impaired development of neural-crest cell-derived organs and intellectual disability caused by MED13Lhaploinsufficiency. Human Mutation, 35(11):1311-20. doi: 10.1002/humu.22636
  4. Lawson JA, Chan CF, Chi CS, Fan PC, Kim HD, Tay SK, . . . Tham CK (2013). Managing tuberous sclerosis in the Asia-Pacific region: Refining practice and the role of targeted therapy. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia, 21(7):1180-7. doi: 10.1016/j.jocn.2013.06.029
  5. Krieger M, Roos A, Stendel C, Claeys KG, Sonmez FM, Tay SK, . . . Senderek J. SIL1 mutations and clinical spectrum in patients with Marinesco-Sjogren syndrome. Brain : a journal of neurology, 136(Pt 12):3634-44. doi: 10.1093/brain/awt283



Contact

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+65 6779 7486