Associate Chief Physician, Deputy Director of the Clinical Research Ward. Specialties: Long-term engagement in clinical practice and research on pediatric endocrine disorders, inherited metabolic diseases and rare diseases, with a solid and profound professional background and extensive diagnosis and treatment experience. In the field of pediatric endocrinology, he is skilled in diagnosing and treating common and complex refractory endocrine diseases including childhood obesity and abnormal glucose metabolism, various types of hypoglycemia, pediatric diabetes, thyroid diseases, adrenal diseases, short stature, growth retardation, precocious puberty and disorders of sexual development. He has formulated precise, systematic and long-term sustainable management plans for a large number of child patients. In the field of inherited metabolic and rare diseases, he is committed to the early identification, precise diagnosis and exploration of innovative therapies for complex rare genetic disorders and inherited metabolic diseases.

Main research directions: Focusing on innovative diagnosis and treatment of inherited metabolic diseases and rare diseases to improve their early and precise diagnosis, and conducting clinical exploration and research on cutting-edge therapeutic strategies such as gene therapy. Devoted to basic and clinical research on obesity and abnormal glucose metabolism, with emphasis on insulin secretion and its regulatory mechanisms, so as to provide evidence for scientific evaluation and standardized management of metabolic diseases.