1Chinese expert consensus on clinical rehabilitation practice in childhood dystoniaThe Subspecialty Group of Rehabilitation,the Society of Pediatrics,Chinese Medical AssociationGUIDELINES,STANDARDS AND CONSENSUS1-152Paying attention to the identification and treatment of dystonia in childrenLI Ting-song, XIAO NongEDITORIAL16-183Clinical and rehabilitation progress of hereditary spasticJIANG Hong-fang, YU Yong-lin, RUAN Wen-congSYMPOSIUM19-234Clinical and rehabilitation progress of benign paroxysmal torticollis in infancyHAN Ming-shan, XU Kai-shouSYMPOSIUM23-265Research progress of dystonia in dyskinetic cerebral palsy in childrenZHU Deng-na, QIAO Lu-sha, ZHANG Guang-yuSYMPOSIUM26-306Clinical and rehabilitation progress of dopa-responsive dystonia in childrenHOU Mei, SUN Dian-rongSYMPOSIUM30-357Clinical and rehabilitation progress of functional movement disorders in childrenYANG Jia-wen, ZHOU Hao-qin, ZHANG HuiSYMPOSIUM35-408Application value of WPPSI-Ⅳ language comprehension index in the assessment of language ability in children with autism spectrum disorderZHAO Jin-zhu, TANG Li-na, HE Tian-yiORIGINAL CONTRIBUTION41-44,579Genetics and clinical characteristics of epilepsy associated with 1p36 deletion syndrome in 13 casesCHENG Miao-miao, YANG Ying, NIU Xue-yangORIGINAL CONTRIBUTION45-5110Expression and significance of CD25 in peripheral blood in purpura nephritisYU Shi-han, MA Xiao-xue, WEI TongORIGINAL CONTRIBUTION52-5711Research progress in newborn screening for severe combined immunodeficiency,X-linked agammaglobulinemiaCHEN Chi, ZHANG Chao, ZHOU DuoREVIEW58-6312Diagnosis,treatment and management of epilepsy comorbid with tic disorders in childrenLIN Hai-sheng, CHEN Wen-xiongREVIEW64-6913Classical homocystinuria caused by CBS gene mutation:A case report and literature reviewFU Xiao-hui, WU Fei-fei, CUI DongCASE REPORT70-7314A case of multiple carpotarsal osteolysis syndrome with nephrotic syndromeZHANG Hai-mei, ZHANG Hong-xia, LIU Xue-meiCASE REPORT74-7615A case of spinal muscular atrophy with respiratory distress type 1 caused by IGHMBP2 gene variation and literature reviewGE Lin, FANG FangCASE REPORT77-80 