Lead of the Multidisciplinary Team (MDT) for Complex Rare Diseases & Birth Defects Lead of the Genetic Counseling Platform for Clinical Molecular Genetics Center
Academic Rank:Chief Physician
Education:Master Degree
Specialize in the diagnosis and treatment of congenital hypothyroidism, phenylketonuria, G6PD, amino acid metabolism disorders, organic acid metabolism disorders, fatty acid metabolism disorders, mitochondrial diseases, DMD, as well as providing genetic counseling for newborn screening and multidisciplinary team (MDT) management for complex and rare diseases.
Congenital hypothyroidism; Inborn Errors of Metabolism;
newborn screening
Birth Defect Intervention Committee, Neonatologists Branch of Chinese Medical Association (CMA)Vice Chairman
Birth Defect Intervention Committee of Zhejiang Preventive Medicine AssociationVice Chairman
