ABSTRACT
Objective To analyze the epidemiological characteristics and trends of accidental death among children under 5 in Wenzhou during the period of 2007—2016, and to provide basis for the intervention program of accidental death in children. Methods The accidental death case of children in Wenzhou during 2007—2016 were collected,then the variation intensity, trend, and cause of death spectrum of accidental death were analyzed. Results The accidental death rate of children under 5 in this city showed a downward trend (P<0.05) during 2007—2016, with 12.38 per ten thousand on average. The accidental death rate of children in rural area was 13.26 per ten thousand, which was higher than 9.99 per ten thousand in urban area (P<0.05) . The accidental death gap between urban and rural children was narrowed down (P<0.05) . The unintentional death rate of floating children was 18.56 per ten thousand, and was higher than that of local children which was 9.44 per ten thousand (P<0.05) . The first cause of accidental death in children under 5 was accidental asphyxia, but drowning (46.38%) was more prominent in the 1-4 year old children. Conclusion In Wenzhou, the first cause of accidental death in children under 5 was accidental asphyxia.The accidental death of migrant children was significantly higher than local children.These characteristics have a good directional effect on future intervention measures.
ABSTRACT
Objective To carry out mutation analysis of deafness-associated genes for deaf newborns and their parents, and to estimate the recurrence risk for their parents to have deaf descendants.Methods Suspected cases of inherited deafness were identified by neonatal hearing screening and questionnaires. Genomic DNAs of suspected cases and their parents were extracted from their peripheral blood samples . Common deafness-associated genes(i.e. GJB2,SLC26A4 and 12S rRNA genes)were amplified by polymerase chain reaction(PCR),and those PCR products were sequenced for the mutation analysis.Results From 2013 to 2016, 193 cases of deafness were found in neonatal hearing screening,29 cases of suspected as hereditary deafness were screened,and 17 out of 29 cases were found to have mutations in deafness-associated genes(detection rate:58.62%). GJB2 homozygous mutations were identified in two cases and their parents,and the recurrence risk to have deaf descendants was 100%. Four cases of suspected hereditary deafness had GJB2 homozygous mutations,and their parents were both GJB2 mutation carriers. There was one case with SLC26A4 homozygous mutations,and their parents were both SLC26A4 mutation carrier. Two cases were detected to have GJB2 V371 homozygous mutations,and their parents were both GJB2 V371 mutation carriers. For those seven parents carrying deafness-associated mutations above,the recurrence risk of deafness for their descendants was 25%.Conclusion In addition to hearing screening,the genetic diagnosis of deafness-associated genes is helpful to clarify the cause of suspected neonatal hereditary deafness,and can provide objective reproductive counseling and guidance for those deaf parents or parents with deaf children.