Dr. Fong Nai Chung - Paediatrics
Specialist in Paediatrics
Highlights
- MCHK RegisteredVerified
- Specialist in PaediatricsBachelor of Medicine and Bachelor of Surgery (MBChB) · Member of the Royal Colleges of Physicians of the United Kingdom · Fellow of the Hong Kong College of Paediatricians · Medical degree 1991
- InsuranceBeing compiled｜See details
About
Dr. Fong Nai Chung is a registered Paediatrics specialist in Hong Kong.
Education
Specialist in Paediatrics
- Bachelor of Medicine and Bachelor of Surgery (MBChB)Bachelor of Medicine and Bachelor of Surgery (MBChB)1991
- Member of the Royal Colleges of Physicians of the United KingdomMember of the Royal Colleges of Physicians of the United Kingdom1994
- Fellow of the Hong Kong Academy of Medicine (Paediatrics)Fellow of the Hong Kong Academy of Medicine (Paediatrics)1998
- Master of Medical ScienceMaster of Medical Science2001
Hong Kong Academy of Medicine fellowships
- FHKCPaedFellow, Hong Kong College of Paediatricians1998
Source: Hong Kong Academy of Medicine Fellows Register, checked 12 Sep 2026
Locations
Department of Paediatrics Princess Margaret Hospital 2-10 Princess Margaret Hosp Rd Lai Chi Kok Kowloon
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FAQ
Is Dr. Fong Nai Chung any good?
Dr. Fong Nai Chung is a registered Paediatrics specialist in Hong Kong. Qualifications and registration come from the Hong Kong Medical Council. ok.med does not rate or rank doctors.
What does Dr. Fong Nai Chung do?
Dr. Fong Nai Chung practises in Paediatrics.
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ClaimResearch and publications
6 papers
Filter by paper topic
Topics come from medical classifications on these PubMed papers, not from the doctor's listed services.
- Novel finding of lissencephaly and severe osteopenia in a Chinese patient with SATB2-associated syndrome and a brief review of literature.American journal of medical genetics. Part A · 2022
- Left ventricular stiffness in paediatric patients with end-stage kidney disease.Pediatric nephrology (Berlin, Germany) · 2020
- Centrosome-associated CDC25B is a novel disease-causing gene for a syndrome with cataracts, dilated cardiomyopathy, and multiple endocrinopathies.Clinica chimica acta; international journal of clinical chemistry · 2020
- Clinical whole-exome sequencing reveals a common pathogenic variant in patients with CoQ<sub>10</sub> deficiency: An underdiagnosed cause of mitochondriopathy.Clinica chimica acta; international journal of clinical chemistry · 2019
- Diagnostic yield of array CGH in patients with autism spectrum disorder in Hong Kong.Clinical and translational medicine · 2016
- Clinical whole-exome sequencing reveals a novel missense pathogenic variant of GNAO1 in a patient with infantile-onset epilepsy.Clinica chimica acta; international journal of clinical chemistry · 2015
Publication data comes from PubMed / Europe PMC and is matched automatically by name and affiliation. Every entry links to the source.
For reference only. Not medical advice. Read full disclaimer