Research areas : Basic and clinical research on pediatric neuromuscular diseases; precision diagnosis and treatment of rare pediatric neurogenetic diseases. Cutting-edge technologies: Focusing on gene diagnostic research for early-onset muscular dystrophy in children, providing precise guidance for the diagnosis and treatment of similar patients; promoting the establishment of joint clinics for neurological diseases and stem cell transplantation, exploring new pathways for stem cell therapy of neurological diseases; conducting multidisciplinary diagnosis and treatment of pediatric neuromuscular diseases, providing long-term comprehensive management for patients with rare diseases.

Specialties: Spinal muscular atrophy (SMA), Duchenne/Behnken muscular dystrophy, congenital myopathy, inherited metabolic neuropathies, and rare neurological diseases. Academic Highlights: Director of the Asia-Oceania Myopathy Center, Standing Committee Member of the Rare Diseases Branch of the Chinese Medical Association, Deputy Head of the Endocrinology, Genetics and Metabolism Group of the Pediatrics Branch of the Chinese Medical Association, Chairperson of the Rare Diseases Committee of the Chinese Women Physicians Association, Standing Committee Member and Head of the Pediatric Neuromuscular Diseases Group of the Rare Diseases Branch of the Beijing Medical Association; Recipient of a major award for precision diagnosis and treatment technology for early-onset muscular dystrophy.