期刊文献+

眼-脑-肾综合征治疗的回顾性分析(附4例报告) 被引量:2

A RETROSPECTIVE ANALYSIS OF MANAGEMENT RESULTS OF OCULOCEREBRORENAL SYNDROME (A REPORT OF 4 CASES)
下载PDF
导出
摘要 目的 :阐述 4例 (8眼 )眼 脑 肾综合征伴有双侧白内障患者的治疗。方法 :回顾性评论。结果 :2例眼 脑 肾综合征患者首次眼科检查时 ,有肉眼可见双侧白内障 ,所有患者都进行了双眼白内障手术。白内障 (8眼 )摘除时平均年龄是 1 5 (1~ 4 )个月。青光眼的诊断和治疗差别较大。诊断青光眼 (7眼 )时的平均年龄是 33 7(1 0 0~ 70 0 )个月。所有眼都进行了随访 ,随访时间平均 5 1 2 (4 2~ 1 90 )个月。结论 :眼 脑 肾综合征患者应及早鉴别并手术摘除白内障 ;必须严密观察病人眼内压、眼底和屈光度的变化 。 Objective:To analyze the management results in 4 patients with oculocerebrorenal syndrome Method:Retrospective review Results:Two cases of oculocerebrorenal syndrome had visually bilateral cataracts on their first full ophthalmic examination All underwent bilateral cataract surgery The mean age (of 8 eyes) at extraction was 1 5(1~4) months The mean age (of 7 eyes) at glaucoma diagnosis was 33 7 (10~70) months All eyes were followed up for an average of 51 2 months Conclusions:Early identification and surgical removal of cataracts is recommended in patients with oculocerebrorenal syndrome Patients should be monitored closely and regularly for changes in intraocular pressure,optic nerve cupping,and refractive error to rule out the development of glaucoma
出处 《滨州医学院学报》 2004年第5期330-331,共2页 Journal of Binzhou Medical University
关键词 眼-脑-肾综合征 白内障 青光眼 oculocerebrorenal syndrome cataract glaucoma
  • 相关文献

参考文献3

  • 1Cibis GW, Waeltermann JM ,Whitcraft CT,et al. Lenticular opacities in carriers of Lowe's syndrome[J]. Ophthalomology, 1986,93:1041
  • 2Silver DN, Lewis RA, Nussbaum RL. Mapping of the Lowe oculocerebrorenal syndrome to Xq24-q26 by use of restriction fragment length polymorphisms[ J ]. J Clin Invest, 1987,79:282
  • 3Lavin CW, Mckeown CA. The oculocerebrorenal syndrome of Lowe [J]. Int Ophthalmol C1in,1993,33:179

同被引文献12

  • 1洪婕,李秀珍,陶建平.眼-脑-肾综合征1例报道[J].国际医药卫生导报,2007,13(2):56-57. 被引量:2
  • 2诸福棠.实用儿科学[M]7版[M].北京:人民卫生出版社,2002.1833.
  • 3Loi M. Lowe syndrome[J]. Orphanet J Rare Dis,2006,1:16.
  • 4Cau M, Addis M, Congiu R, et al. A locus for familial skewed X chromosome inactivation maps to chromosome Xq25 in a family with a female manifesting Lowe syndrome [ J ]. J Hum Genet, 2006,51 ( 11 ) :1030-1036.
  • 5Hou XM, Hagemann N, Schoebel S, et al. A structural basis for Lowe syndrome caused by mutations in the Rab-binding domain of OCRL1 [J]. EMBO J,2011,30(8) :1659-1670.
  • 6Satre V,Monnier N, Berthoin F, et al. Characterization of a germline mosaicism in families with Lowe syndrome, and identifieation of sev- en novel mutations in the OCRLI gene[ J]. Am J Hum Genet, 1999, 65( 1 ) :68-76.
  • 7Tasic V, Lozanovski VL, Korneti P, et al. Clinical and laboratory fea- tures of Macedonian children with OCRL mutations J 1. Pediatr Neph- ro1,2011,26 ( 4 ) :557-562.
  • 8Ruellas AC, Pithon MM, Oliveira DD, et al. Lowe syndrome : litera- ture review and case report [ J ]. J Orthod ,2008,35 ( 3 ) : 156 -60.
  • 9史湘舟,崔占杰,蒲方,夏红见.眼—脑—肾综合征合并半乳糖血症1例[J].疑难病杂志,2013,12(7):556-556. 被引量:1
  • 10赵爱英.肾综合征出血热54例误诊分析[J].临床误诊误治,2000,13(6):411-411. 被引量:1

引证文献2

二级引证文献3

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部