期刊文献+

Kallmann综合征的影像学表现 被引量:3

在线阅读 下载PDF
导出
摘要 目的提高Kallmann综合征(KS)的影像学诊断水平。方法回顾性分析2例KS患者的临床资料、腕关节X线片和头颅MR影像学特点。结果2例均表现为性发育迟缓,第二性征缺乏,嗅觉障碍;X线片提示腕部骨骺发育迟缓,骨龄延迟;MR冠状面T1WI和T2WI均发现嗅球、嗅束缺如,嗅沟消失。结论KS的影像表现具有一定特征性,能为临床诊断提供重要的依据;临床应注意对KS与Klinefelter综合征进行鉴别。
出处 《山东医药》 CAS 北大核心 2009年第7期77-79,共3页 Shandong Medical Journal
  • 相关文献

参考文献6

  • 1郝丽君,崔英霞,王云华,商学军,黄宇烽.Kallmann综合征的诊断与鉴别诊断[J].中华男科学杂志,2005,11(10):765-766. 被引量:9
  • 2邓春华,梅骅,苗永青.Kallmann 综合征四例报告[J].中华泌尿外科杂志,1997,18(5):298-300. 被引量:13
  • 3王伟.Kallmann综合征的临床诊治[J].中国实用儿科杂志,2006,21(7):485-487. 被引量:3
  • 4Knott JR, Ragland RL, Brown RS, et al. Kallmann syndrome: MR findings[J]. AJNR,1993,14(4) :845-851.
  • 5Vogl T J, Stemnler J, Heye B,el al. Kallmann syndrome versus idio-pathic hypogonadotropic hypogonadism at MR imaglng[J]. Radiology, 1994,191 ( 1 ) :53-57.
  • 6Yousem DM, Geckle RJ, Bilker W, et al. MR evaluation of patients with congenital hyposmia or anosmla[ J ]. AIR, 1996,166 (2) :439- 443.

二级参考文献10

  • 1邓春华,梅骅,苗永青.Kallmann 综合征四例报告[J].中华泌尿外科杂志,1997,18(5):298-300. 被引量:13
  • 2Madan R, Sawlani V, Gupta S, et al. MRI findings in Kallmann syndrome[J]. Neurol India, 2004,52(4) :501-503.
  • 3Rugarli EI,Ballabio A. Kallmann syndrome:From genetics to neurobiology[J]. JAMA, 1993, 270(22) :2713-2716.
  • 4Voorhoeve PG, Delemarre-van de Waal HA. From gene to disease: hypogonatrophic hypogonadism and anosmia: Kallmann's syndrome[ J ]. Ned Tijdschr Geneeskd, 2004, 148 ( 23 ): 1142-1144.
  • 5史轶繁.协和内分泌和代谢学[M].北京:科学出版社,1999.1020-1021.
  • 6Bick D, Franco B, Sherins R J, et al. X chromosome-linked Kall-mann syndrome:stop mutations validate the candidate gene [ J ].N Engl J Med, 1992,36 : 1752-1755.
  • 7Oliveira LMB, Seminara SB, Beranova M, et al. The importance of autosomal genes in Kallmann syndrome:genotype-phenotype correlations and neuroendocrine characteristics. J Clin Endocr[ J ].Metab ,2001,86 : 1532-1538.
  • 8Iovane A, Aumas C, de Roux N. New insights in the genetics of isolated hypogonadotropic hypogonadism [ J ]. Eur J Endocrinol,2004,151(3) :83-88.
  • 9de Roux N. Isolated gonadotropic deficiency with and withour anosmia:a developmental defect or a neuroendocrine regulation abnormality of the gonadotropic axis[ J]. Horm Res,2005,64 ( 2 ) :48-55.
  • 10Pitteloud N, Aciemo JS Jr, Meysing A, et al. Mutations in fibroblast growth factor receptor 1 cause both Kallmann syndrome and normosmic idiopathic hypogonadotrepic hypogonadis [ J ]. Proc Natl Acad Sci USA,2006,103:6281-6286.

共引文献19

同被引文献24

引证文献3

二级引证文献5

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