1Consensus on diagnosis and treatment of childhood vasculitis in China:Kawasaki diseaseAcademic Group of Pediatric Rheumatology and Immunology,Society of Pediatrics,Chinese Medical Doctor AssociationGUIDELINES,STANDARDS AND CONSENSUS481-4882Consensus on diagnosis and treatment of childhood vasculitis in China:ANCA-associated vasculitisAcademic Group of Pediatric Rheumatology and Immunology,Society of Pediatrics,Chinese Medical Doctor AssociationGUIDELINES,STANDARDS AND CONSENSUS489-4973Current status and tendency of neonatal genetic screeningZHANG Jin-man, ZHANG Yin-hong, HAN Lian-shuEDITORIAL498-5014Emphasizing the diagnosis and treatment concept of ingestive trauma in childrenFANG YingEDITORIAL502-5055Multiomics technology for screening of genetic metabolic diseases in newbornsZOU Hui, GUO Yuan-fangSYMPOSIUM506-5106Importance of multidisciplinary diagnosis and treatment in neonatal screeningHUANG Yong-lanSYMPOSIUM510-5137Management of positive screening and confirmed patients with neonatal genetic metabolic diseasesYANG Ru-lai, SHU QiangSYMPOSIUM513-5168Interpretation of the expanded newborn screening results for inborn errors of metabolism by tandem mass spectro-metryLIANG Li-liSYMPOSIUM516-5209Current screening,diagnosis and treatment of phenylketonuria in neonatesWANG Xiao-huaSYMPOSIUM520-52410Analysis of body composition and risk factors of non-alcoholic fatty liver disease in obese childrenLI Dong-dan, YAN Jie, WANG Mei-chenORIGINAL CONTRIBUTION525-52911Clinical characteristics of Beh?et's syndrome in children:An analysis of 33 casesCHEN Feng-hua, AN Yun-fei, TANG Xue-meiORIGINAL CONTRIBUTION530-535,54012Progress in the diagnosis and treatment of Sotos syndromeLUO Tian, WANG Yi, ZHOU Shui-zhenREVIEW AND LECTURE536-54013Research progress in phenotypes and treatments of KCNMA1-related neurologicaI disordersTIAN Xiao-juan, DING Chang-hongREVIEW AND LECTURE541-54414Progress of associated factors of sleep disorders in children with autism spectrum disordersCHEN Meng-xiang, GUO Lan-min, XING XiaoREVIEW AND LECTURE545-55015Perampanel in the treatment of Dravet syndrome:A case report and literature reviewLUO Xu-feng, LUO Zhi-qiang, LI Yong-liCASE REPORT551-55416Clinical characteristics of 3 cases of mental retardation caused by CTNNB1 gene mutation and the literature reviewCHEN Shu-juan, SONG Jia-li, XIN Qing-gangCASE REPORT555-560 