罕见病作为一类高度异质性且复杂的疾病,日益受到广泛的关注。此类疾病具有诊断难、治疗难和研究难的特点,对患者及其家庭的生活质量造成严重影响。近年来,罕见病的发病机制研究和诊疗技术取得了令人瞩目的进展。为促进国际学术交流,推动基础研究向临床转化的创新发展,中国神经科学学会神经病学基础与临床分会将于2026年10月29日至11月1日在浙江省杭州市举办首届“神经系统罕见病国际研讨会”。
本次会议由浙江大学医学院附属第二医院医学遗传科/罕见病诊治中心承办,会议聚焦运动障碍疾病的发病机制、临床诊断与基因治疗进展,将系统探讨其分子病理机制、精准诊断策略及前沿基因治疗应用,为患者提供更精准高效的诊疗方案。会议将邀请国内外专家进行专题讲座和学术交流,分享最新研究成果与诊疗经验。
Highly heterogeneous and complex, rare diseases have drawn increasing attention worldwide. Difficulties in diagnosis, treatment and research greatly affect the life quality of patients and their families. Recent years have witnessed impressive advances in the pathogenesis, diagnosis and treatment of rare diseases.
To boost international academic communication and promote the translation of basic research into clinical application, the Basic and Clinical Neurology Branch of Chinese Society for Neuroscience will host the inaugural International Conference on Rare Neurological Diseases (ICRND 2026) in Hangzhou, Zhejiang, from October 29 to November 1, 2026.
Organized by the Department of Medical Genetics & Rare Disease Diagnosis and Treatment Center, the Second Affiliated Hospital of Zhejiang University School of Medicine, the conference centers on movement disorders, covering their pathogenesis, clinical diagnosis and latest gene therapy progress. It will explore molecular pathology, precision diagnosis and innovative gene therapies to optimize clinical care for patients. Distinguished experts from across the globe will share cutting-edge research and clinical expertise through lectures and discussions.