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Dr Chin Hui-Lin

Photo of Dr Chin Hui-Lin
MBBS (S'pore), MMed (Paeds) (S'pore), MRCPCH (UK), MCI
Consultant, Division of Paediatric Genetics & Metabolism, Department of Paediatrics, Khoo Teck Puat - National University Children's Medical Institute, National University Hospital
Sub Specialty:
Paediatric Genetics and Metabolism
Medical and Surgical Conditions:
Atrial Septal Defect (Children), Autism (Children), Congenital Heart Conditions (Newborn), Disorders of Sex Development (Children), G6PD Deficiency (Children), Growth Disorders in Children, Haemophilia (Children), Handwriting Difficulty (Children), Hearing Loss (Children), Inborn Errors of Metabolism, Marfan Syndrome (Children), Paediatric Cataracts, Turner Syndrome (Children), Universal Hearing Screening Programme
National University Hospital
National University Health System
Dr Chin Hui-Lin is a paediatrician with training in the field of Genetics and Metabolism. She graduated from Yong Loo Lin School of Medicine, National University of Singapore, with the Jane Prize in Paediatrics and was in the pioneer batch of the Paediatric Residency Programme at the National University Healthcare System. She obtained her Master of Medicine (Paediatrics) and membership of the Royal College of Paediatrics and Child Health in 2014. She has since completed her Specialist Accreditation for Paediatric Medicine and also obtained a Masters in Clinical Investigation.

Dr Chin contributes actively to undergraduate and postgraduate medical education. She has been awarded the Dean’s award for Teaching Excellence as well as received the Dean’s Office Junior Doctor Teaching Award and teaching awards from the Department of Paediatrics on multiple occasions. Dr Chin also contributes to research in the field of genetics and rare diseases.

Research and Publications

  1. Chang X, Chin HL, Quek SC, Goh DY, Dorajoo R, Friedlander Y, Heng CK (2017). The genetic variation rs6903956 in the novel androgen-dependent tissue factor pathway inhibitor regulating protein (ADTRP) gene is not associated with levels of plasma coagulation factors in the Singaporean Chinese. Thrombosis Journal, 15:1. doi: 10.1186/s12959-016-0124-y
  2. Chin HL, Aw MM, Quak SH, Huang J, Hart CE, Prabhakaran K, Goh DL (2015). Two consecutive partial liver transplants in a patient with Classic Maple Syrup Urine Disease. Molecular Genetics and Metabolism Reports, 4:49-52. doi: 10.1016/j.ymgmr.2015.06.003


Appt Tel:
+65 6779 7486