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Goldmann-Favre综合征一例 被引量:1

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摘要 患者男性,57岁?因双眼夜盲、畏光5年余于2013年3月1日于首都医科大学附属北京同仁医院北京同仁眼科中心就诊。患者3年前双眼行门内障摘除术。否认其他病史,否认家族病史。
出处 《中华眼科杂志》 CAS CSCD 北大核心 2016年第1期60-62,共3页 Chinese Journal of Ophthalmology
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参考文献12

  • 1Madhavendra Bhandafi, Rajni Rajah, Tandava Kristman, et al. Morphological and functional correlates in Goldmann-Faw'e syndrome: a case series[J]. Korean J Ophthahnol, 2012, 26(2): 143-146. DOI: 10. 3341/kjo. 2012.26.2. 143. 被引量:1
  • 2Theodossiadis PG, Koutsandrea C, Kollia AC, et al. Optical coherence tomography in the study of the Goldmann-Favre syndronle [J]. Am J Ophlhahnol, 2000, 129(4): 542- 544. 被引量:1
  • 3王凯,黎晓新,姜燕荣.Goldmann—Favre综合征二例[J].中华眼科杂志,2008,44(9):847-850. 被引量:3
  • 4Pachydaki SI, Klaver CC, Barbazetto IA, et al. Phenolypic features of patients with NR2E3 mutations[J]. Arch Ophthalmol, 2009, 127(1): 71-75. 被引量:1
  • 5Peyman GA, Fishman GA, Sanders DR, et al. Histopathology of Goldmann-Favre syndrome obtained by full-thickness eye- wall biopsy[J]. Ann Ophthalmol, 1977, 9(4): 479-484. 被引量:1
  • 6陈跃,皮敏石.斯蒂克勒综合征5例分析[J].福建医科大学学报,2000,34(2):154-156. 被引量:3
  • 7Udar N, Small K, Chalukya M, et al. Developmental or degenerative--NR2E3 gene mutations in two patients with enhanced S cone syndrome[J]. Mol Vis, 2011, 17: 519-525. 被引量:1
  • 8Sharon D, Sandberg MA, Caruso RC, et al. Shared mutations in NR2E3 in enhanced S-cone syndrome, Goldmann-Favre syndrome, and many cases of clumped pigmentary retinal degeneration[J]. Arch Ophthalmol, 2003, 121(9): 1316-1323. 被引量:1
  • 9Marmor MF. A teenager with nightblindness and cysticmaculopathy: enhanced S cone syndrome(Goldmann-Favre syndrome)[J]. Doc Ophthalmol, 2006, 113(3): 213-215. 被引量:1
  • 10Sidiki SS, Hamilton R, Dutton G N. Fear of the dark in children: is stationary night blindness the cause[J]. BMJ, 2003, 326(7382): 211-212. 被引量:1

二级参考文献26

  • 1睢瑞芳,赵家良.先天性静止性夜盲[J].中华眼科杂志,2006,42(5):472-475. 被引量:8
  • 2Nasr YG, Cherfan GM, Michels RG, et al. Goldmann-Favre maculopathy. Retina, 1990,10:175-180. 被引量:1
  • 3Fishman GA, Jampol LM, Goldberg MF. Diagnostic features of the Goldmann-Favre syndrome. Br J Ophthalmol, 1976,60:345- 353. 被引量:1
  • 4Green JL Jr, Jampol LM. Vascular opaeiflcation and leakage in X- linked (juvenile) retinoschisis. Br J Ophthalmol, 1979,63:368- 373. 被引量:1
  • 5Chavala SH, Sail A, Lewis H, et al. An Arg311Gln NR2E3 mutation in a family with classic Goldmann-Favre syndrome. Br J Ophthalmol, 2005,89 : 1065-1066. 被引量:1
  • 6Izumi K, Matsuhashi M. Goldmann-Favre syndrome in a four- year-old-girl. Doc Ophthalmol, 1987,66:219-226. 被引量:1
  • 7Jacobson SG, Roman AJ, Roman MI, et al. Relatively enhanced S-cane function in the Goldmann-Favre syndrome. Am J Ophthalmol, 1991,111:446-453. 被引量:1
  • 8Peyman GA, Fishman GA, Sanders DR, et al. Histopathology of Goldmann-Favre syndrome obtained by full-thickness eye-wall biopsy. Ann Ophthalmol, 1977,9:479-484. 被引量:1
  • 9Fishman GA, Fishman M, Maggiano J. Macular lesions associated with retinitis pigmentosa. Arch Ophthalmol, 1977,95:798-803. 被引量:1
  • 10Marmor MF. A teenager with nightblindness and cystic maculopathy: Enhanced S-cone syndrome (Goldmann-Favre syndrome). Doc Ophthalmol, 2006,113:213-215. 被引量:1

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