Deputy Director of the Shanghai Institute of Pediatric Medicine, Academic Leader of Pediatric Endocrinology, Genetics and Metabolism, Chief Physician, Level 2 Dr., Doctoral Supervisor, and Expert Receiving Special Government Allowances from the State Council
Affiliated HospitalXinhua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine
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Member of the Expert Committee on Rare Disease Diagnosis and Treatment and Guarantee of the National Health and Family Planning Commission, Vice President of the Medical Genetics Physician Branch of the Chinese Medical Doctor Association, and Head of the Neonatal Disease Screening Group of the Child Health Branch of the Chinese Preventive Medicine Association. Since 1981, he has been deeply involved in the research of genetic metabolic diseases, pioneering neonatal genetic metabolic disease screening in China, establishing multiple detection technologies for the differential diagnosis of phenylketonuria, and formulating multiple industry standards. He specializes in amino acid metabolic diseases such as phenylketonuria, organic acid metabolic diseases such as methylmalonic acidemia, mucopolysaccharidosis, lysosomal diseases such as Gaucher disease, and multiple malformation syndromes. He has trained over ten thousand neonatal screening laboratory technicians and clinicians, benefiting millions of newborns nationwide.