期刊文献+

Bardet-Biedl综合征一例 被引量:1

原文传递
导出
摘要 患者男性,18岁.因双眼自幼渐进性视力下降伴夜盲,于2012年10月17日在首都医科大学附属北京同仁医院北京同仁眼科中心就诊.患者面容呆滞(图1),自幼肥胖,智力低下,情绪不稳,5岁学会说话,12岁进入特殊学校,韦氏儿童智力量表检查显示智商26分,精神发育迟滞(中度偏重).因先天性心脏病、房间隔缺损、三尖瓣轻度关闭不全,于2009年12月在外院行房间隔缺损修补手术;2011年11月因下消化道出血、肛裂于外院治疗;2012年9月因患胆囊结石、急性胃肠炎于外院治疗.否认结核、伤寒、肝炎等传染病史.
出处 《中华眼科杂志》 CAS CSCD 北大核心 2013年第11期1035-1037,共3页 Chinese Journal of Ophthalmology
  • 相关文献

参考文献15

  • 1Guo DF, Rahmouni K. Molecular basis of the obesity associated with Bardet-Biedl syndrome. Trends Endocrinol Metab, 2011,22 : 286-293.
  • 2Beales PL, Elcioglu N, Woolf AS, et al. New criteria for improved diagnosis of Bardet-Biedl syndrome : results of a population survey. J Med Genet, 1999,36:437-446.
  • 3Muller J,Stoetzel C, Vincent MC, et al. Identification of 28 novel mutations in the Bardet-Biedl syndrome genes: the burden of private mutations in an extensively heterogeneous disease. Hum Genet,2010,127:583-593.
  • 4郑湘榕,尹飞,黄榕,向秋莲.Bardet-Biedl综合征1例[J].中国当代儿科杂志,2011,13(7):602-603. 被引量:5
  • 5陈皆春,李成武,高健生,刘海光.Bardet-Biedl综合征3例[J].中国中医眼科杂志,2008,18(1):38-40. 被引量:5
  • 6Lee JE, Gleeson JG. Cilia in the nervous system: linking cilia function and neurodevelopmental disorders. Curr Opin Neurol, 2011,24:98-105.
  • 7Forsythe E, Beales PL. Bardet-Biedl syndrome. Eur J Hum Genet, 2013,21:8-13.
  • 8Sowjanya B, Sreenivasulu U, Naidu JN, et al. End stage renal disease, differential diagnosis, a rare genetic disorder: bardet-biedl syndrome: case report and review. Indian J Clin Biochem,2011, 26:214-216.
  • 9林东晓,陈钢锋,瞿佳.Bardet-Biedl综合征一例[J].中华眼科杂志,2007,43(2):174-175. 被引量:3
  • 10Buscher AK, Cetiner M, Buscher R, et al. Obesity in patients with Bardet-Biedl syndrome : influence of appetite-regulating hormones. Pediatr Nephro1,2012,27:2065-2071.

二级参考文献29

  • 1Beales PL, Elcioglu N, Woolf AS, Parker 1), Flinter FA. New criteria for improved diagnosis of Bardet-Biedl syndrome : results of a population survey[J]. J Med Genet, 1999, 36(6) :437-446.
  • 2Muller J, Stoetzel C, Vincent MC, Leitch CC, Laurier V, Danse JM, et al. Identification of 28 novel mutations in the Bardet-Biedl syndrome genes: the burden of private mutations in an extensively heterogeneous disease[J]. Ham Genet, 2010, 127(5) :583-593.
  • 3Lee JE, Gleeson JG. Cilia in the nervous system: linking cilia function and neurodevelopmental disorders [ J ]. Curr Opin Neu- rol, 2011, 24(2) :98-105.
  • 4Katsanis N, Lupski JR, Beales PL. Exploring the molecular basis of Bardet-Biedl syndrome[ J 1. Hum Mol Genet, 2001, 10 (20) : 2293 -2299.
  • 5Putoux A, Attie-Bitach T, Martinovic J, Gubler MC. Phenotypic variability of Bardet-Biedl syndrome : focusing on the kidney[ J]. Pediatr Nephrol, 201l Jan 19. [ Epub ahead of printJ.
  • 6Andrade L.I, Andrade R, Franqa CS, Bittencourt AV. Pigmentary retinopathy due to Bardet-Biedl syndrome: case report and litera- ture review [ J ]. Arq Bras Oftalmol, 2009, 72 ( 5 ) : 694-696.
  • 7Riise R, Andreasson S, Borgastrom MK, Wright AF, Tommerup N, Rosenberg T, et al. Intrafamilial variation of the phenotype in Bardet-Biedl syndrome [ J ]. Br J Ophthahnol, 1997, 81 (5) : 378-385.
  • 8Aloulou H, Cheikhrouhou lq, Belguith N, Ben Ameur S, Ben Mansour L, Chabehoub I, et al. Bardet Biedl syndrome in the child. A study about 11 cases[ J]. Tunis Med, 2011, 89 ( 1 ) : 31- 36.
  • 9Beales PL et al.J Med Genet,1997;34:92-98
  • 10Riise R et al. Br J Ophthalmology,1997;81:378-385

共引文献15

引证文献1

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