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单纯性晶状体异位一家系
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- Author:
- No author available
- Journal Title:
- CHINESE JOURNAL OF OPHTHALMOLOGY
- Issue:
- 6
- DOI:
- 10.3760/j:issn:0412-4081.2004.06.019
- Key Word:
- No keyword available
Abstract： @@ 晶状体异位是指晶状体偏离其在视轴中央的正常位置,包括全异位和半异位两类.该体征可单独出现,如外伤性晶状体异位、先天性晶状体异位,也可为全身病变的一部靠分,如马方综合征.单纯性晶状体异位临床表现不同于马方综合征,除眼部异常外,无骨骼和心血管系统异常;而单纯性晶状体异位与先天性晶状体异位的区别在于前者出生时晶状体位置并无异常.该病在我国至今尚无家系报告.我们在诊治一例儿童病例时,发现了单纯性晶状体异位家系,现报告如下.
- [1]A, Sinha,A, Rahman.Ectopia lentis in a family.[J].1980,28(1).
- [2]M, al-Salem.Autosomal recessive ectopia lentis in two Arab family pedigrees.[J].1990,11(2).
- [3]Tsipouras, P.,Del Mastro, R..Genetic linkage of the Marfan syndrome, ectopia lentis, and congenital contractural...[J].1992,326(14).
- [4]Evans AL,Cooling RJ,Comeglio P,etc.Identification of FBN1 gene mutations in patients with ectopia lentis and marfanoid habitus.[J].2002,86(12).
- [5]C, Ruiz,F, Rivas,V M, Villar-Calvo,etc.Familial simple ectopia lentis. A probable autosomal recessive form.[J].1986,7(2).
- [6]胡诞宁编著.眼科遗传学[M].1988.
- [7]M. J. Edwards,C. J. Challinor,P. W. Colley,etc.Clinical and linkage study of a large family with simple ectopia lentis linked to FBN1[J].1994,53(1).
- [8]D S, Casper,J W, Simon,L B, Nelson,etc.Familial simple ectopia lentis: a case study.[J].1900,22(6).