期刊文献+

家族性高胆固醇血症黄瘤病一例

原文传递
导出
摘要 1临床资料 患者女性,25岁。因全身多发肿物22年于2011年5月来我院门诊就诊。患者于3岁时被发现双手掌指关节伸侧出现隆起于皮肤的皮疹,初与皮肤颜色相近,之后逐渐呈棕黄色,无自觉症状。随年龄增长,四肢各关节的伸侧及屈侧、骶尾部、双侧腋窝及内眦逐渐出现类似肿物(图1—5),增多增大,并融合成片,但无任何不适及关节活动障碍,为改善眼部外观在我院门诊行双侧内眦肿物切除术,术后病理报告为“左内眦、右内眦考虑为睑黄瘤”。患者无高血压、糖尿病、甲亢、肝炎病史及遗传病史,父母非近亲结婚,家族中无类似体征。体检:发育、营养及全身情况良好,各系统检查均未见异常。
出处 《中国美容整形外科杂志》 CAS 2013年第1期35-36,共2页 Chinese Journal of Aesthetic and Plastic Surgery
  • 相关文献

参考文献6

二级参考文献30

  • 1Sibley C, Stone NJ. Familial hypercholesterolemia:A challenge of diagnosis and therapy. Cleve Clin J Med, 2006,73:57-64.
  • 2Wang L, Lin J, Liu S, et al. Mutations in the LDL receptor gene in four Chinese homozygons familial hypercholesterolemia phenotype patients. Nutrition, Metabolism and Cardiovascular Diseases, 9009,19 : 391-400.
  • 3Chen K, Mu YM, Wang BA, et al. Two novel mutations 685del land D129G in the low-density lipoprotein receptor gene in a compound heterozygote Chinese family with familial hypercholesterolemia. Metabolism, 2007,56:636-640.
  • 4Innerarity TL, Mahley RW, Weisgraber KH, et al. Familial defective apolipoprotein B-100:a mutation of apolipoprotein B that causes hypercholesterolemia. J Lipid Res, 1990,31: 1337-1349.
  • 5Abifadel M, Varret M, Rabes JP, et al. Mutations in PCSK9 cause autosomal dominant hypercholesterolemia, Nat Genet, 2003,34: 154-156.
  • 6Damgaard D, Jensen JM, Larsen ML, et al. No genetic linkage or molecular evidence for involvement of the PCSK9, ARH or CYPTA1 genes in the Familial Hypercholesterolemia phenotype in a sample of Danish families without pathogenic mutations in the LDL receptor and apoB genes. Atherosclerosls, 2004,177:415-422.
  • 7Saint Jore B, Varret M, Dachet C, et al. Autosomal dominant type Ⅱ a hypercholesterolemia: evaluation of the respective contributions of LDL-R and apoB gene defects as well as a third major group of defects. Eur J Hum Genet, 2000,8:621-630.
  • 8Tveten K, Ranheim T, Berge KE, et al. Analysis of alternatively spliced isoforms of human LDL receptor mRNA. Clin Chim Acta, 2006,373 : 151-157.
  • 9Peeters AV, Kotze MJ, Scholtz CL, et al. A 3-basepair deletion in repeat 1 of the LDL receptor promoter reduces transcriptional activity in a South Afriean Pedi. J Lipid Res, 1998, 39: 1021- 1024.
  • 10Bertolini S, Cassanelli S, Gamti R, et al. Analysis of LDL receptor gene mutations in Italian patients with homozygous familial hypercholesterolemia. Arterioseler Thromb Vase Biol, 1999,19:408-418.

共引文献4

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