复杂性双侧并指多指并趾畸形一家系五例
摘要
先证者,男,7岁。因双手双足先天畸形入院。身体检查:神志清,智力正常,头面部,胸腹部及脊柱未见异常。左侧隐睾。右手中、环、小指并指畸形,小指多一赘生指。左手中、环指并指畸形合并小指多一赘生指。双足五趾并趾畸形。
出处
《中华小儿外科杂志》
CSCD
北大核心
2008年第1期63-64,共2页
Chinese Journal of Pediatric Surgery
参考文献8
-
1汤熙翔.非综合征型并指(趾)畸形的遗传学研究进展[J].国外医学(遗传学分册),1999,22(5):257-260. 被引量:3
-
2Mc Kusick VA.编著.人类孟德尔遗传.第11版.北京:北京医科大学中国协和医科大学联合出版社,1996.12.
-
3Goodman FR, M undlos S, Muragaki Y. Synpolydactyly phenotypes correlate with size of expansions in HOXD1 3polyalanine tract. Proc Nall Acad Sci USA, 1997,94:7458-7463.
-
4Radhakrishna U,Blouin JL,Mehenni H,et al. Mapping one form of autosomal dominanl postaxial polydactyly type A to chromosome 7p1 5-q1 1.23 by linkage analysis. Am J Hum Genet, 1997, 60 :597-604.
-
5Tsukurov O, Boehmer A. Flynn J. A complex bilateral polysyndactyly disease locus maps to chromosome 7q36. Nat Genet, 1994,6: 282-286.
-
6Vortamp A, Gessler M,Grzeschik KH, et al . GLI3 zinc, finger gene interrupted by translocation in Greig syndrome families. Nature, 1991,352 : 539-540.
-
7Gladwin A,Donnai D,Metcalfe K,el al. Localization of a gene for oculodentodigital syndrome to human chromosome 6 (122-q24. Hum Molec Genet, 1997,6:123-127.
-
8Zhao H, Tian Y, Breedveld G. et al . Postaxial polydactyly type A/13(PAP--A/B)is linked to chromosonle 19p13. 1-13. 2 in a Chinese kindred. Eur J Hum Genel,2002,10:162-166.
-
1手术前后的处理及外科并发症[J].国外科技资料目录(医药卫生),1999(9):40-40.
-
2余江,金铸,文小泉,张辰.先天性并指(趾)畸形治疗体会[J].中国实用外科杂志,2005,25(10):628-628.
-
3周霄.对话专家,探究有疼痛感的心理问题[J].康复,2015,0(5):15-15.
-
4金伟,盖铭文,刘恩煦,孙德骏.少见多趾(指)并趾畸形1例报告[J].中国矫形外科杂志,2008,16(23):1839-1839. 被引量:2
-
5许树林,孙涛,何文涛,钱峰.多跖多趾并短跖短趾及并趾畸形1例[J].中国临床解剖学杂志,2002,20(4):258-258.
-
6枚.男人应学会自检[J].性教育与生殖健康,2001(1):84-85.
-
7CT和核磁哪个更好?[J].健康指南(中老年),2014,0(9):70-70.
-
8刘立新,钟晓云.先天性右足第二、三趾巨趾症合并并趾畸形一例报告[J].赣南医学院学报,1998,18(2):121-121.
-
9有些疼痛可能是“心病”[J].长寿,2016,0(12):46-47.
-
10张静喆.摘除胆囊之后……[J].健康博览,2011(3):25-25.