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中国822例肢体短缩畸形分析 被引量:7

Analysis of 822 Infants with Limb Reduction Defect in China
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摘要 为了解我国肢体短缩畸形(LRD)的基本状况,采用以医院为基础的监测方法,对1986年10月至1987年9月全国29省(市、自治区)945所医院收集的822例LRD围产儿进行了分析。结果表明:全国LRD发生率为6.6/万,云南、贵州、福建和江西省显著高于全国水平(P<0.05),上海市的发生率低于全国水平(P<0.01)。低体重儿中LRD发生率高于正常体重组(P<0.001)。乡村与城镇发生率存在差异(P<0.001),患儿无性别差异。畸形以四肢受累最为常见;上肢受累高于下肢(P<0.001),左右侧无差异(P>0.05)。24.2%的患儿为单发LRD,伴有其它畸形的发生率为75.8%。 This work is aimed at the basic condition of infants with limb reduction defect (LRD) in China.822 cases of LRD occurring among 1243 284 live and stillbirths of 28 or more gestation weeks in China from Oct.1986 to Sept.1987 were analysed.The overall prevalence of LRD was 6.6 per 10000 ranging from 14.4 per 10 000 to 3.6 per 10 000. No sex difference was observed.The prevalence of LRD in infants with low birthweight was significantly higher than that in infants with normal birthweight ( P <0.001).Also the prevalence of LRD in rural area was higher than that in urban area ( P <0 001). Four limb involvement was most common.The cases with only upper limb involvement (278/451,61,6%) were significantly more prevalent than those with only lower limb involvement (173/451,38.4%, P <0 001),but no difference was found between the left LRD and right LRD ( P >0 05),nor was a significant difference noted between single LRD and multiple LRD.75.8% of the infants with LRD had defects in other systems.
出处 《华西医科大学学报》 CSCD 1996年第4期400-404,共5页 Journal of West China University of Medical Sciences
关键词 肢体短缩畸形 围产儿 流行病学 Limb reduction defects Perinatals Epidemiology
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参考文献1

  • 1Xiao K Z,Int J Epidemiol,1990年,19卷,4期,987页

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  • 2代礼,周光萱,朱军,毛萌,衡正昌.中国围产儿并指与并趾畸形的流行病学特征[J].中华妇产科杂志,2004,39(7):436-438. 被引量:8
  • 3朱军,代礼,周光萱,王艳萍,梁娟,缪蕾.1996-2000年全国肢体短缩畸形流行病学分析[J].四川大学学报(医学版),2006,37(5):816-817. 被引量:12
  • 4洪霙,叶江霞,刘捷,黄茵,宋晓红,胡兴照.小儿先天畸形110例种类分析[J].实用儿科临床杂志,2007,22(9):698-700. 被引量:3
  • 5Temtamy SA, McKusick VA. The genetics of hand malformations-Birth defects original article series. New York:Alan R Liss, 1978:53-72.
  • 6Elliott AM, Evans JA, Chudley AE. Split hand foot malformation (SHFM). Clin Genet, 2005 , 68 (6) : 501-505.
  • 7Duijf PH, van Bokhoven H, Brunner HG. Pathogenesis of split-hand/split-foot malformation. Hum Mol Genet, 2003. 12 (Spec No 1):R51-60.
  • 8Elliott AM, Reed MH, Chudley AE, et al. Clinical and epidemiological findings in patients with central ray deficiency: split hand loot malformation (SHFM) in Manitoba, Canada. Am J Med Genet A, 2006 , 140(13) : 1428-1439.
  • 9Kang YS, Cheong HM, Moon Y, et al. Molecular genetic characterization of a Korean split hand/split foot malformation (SHFM). Mol Cells,2004 , 17(3) :397-403.
  • 10Czeizel AE, Vitez M, Kodaj I, et al. An epidemiologieal study of isolated split hand/foot in Hungary, 1975-1984. J Med Genet,1993,30(7) :593-596.

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