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抗血管内皮生长因子药物治疗皮肤色素失禁症相关性视网膜病变一例 被引量:5

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摘要 患儿女,50 d.因“儿科建议筛查眼底”于2013年8月2日来我院眼科门诊就诊.患儿足月顺产,出生体重3000 g,无吸氧史;否认家族遗传病史.患儿出生后躯干、四肢、腋窝处皮肤出现红色斑点、水疱,随后破裂、结痂,色素沉着,儿科诊断为色素失禁症,建议眼科筛查.患儿一般情况良好;全身皮肤点片状色素斑,以腹股沟、腋窝及四肢皮肤多见.口腔科及神经内科检查未见明显异常.
出处 《中华眼底病杂志》 CAS CSCD 北大核心 2015年第1期88-89,共2页 Chinese Journal of Ocular Fundus Diseases
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参考文献8

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同被引文献71

  • 1李莉,宋国维,杜军保,刘吉荣,徐放生,刘晓雁,张霆.色素失禁症NEMOΔ4~10基因片段缺失的初步研究[J].中华儿科杂志,2005,43(2):89-92. 被引量:11
  • 2李莉,宋国维,徐放生,袁新宇,李晓雁,解湘陵,杜军保.色素失禁症15例临床研究[J].中国实用儿科杂志,2005,20(8):472-474. 被引量:19
  • 3宋哲,黎晓新.皮肤色素失禁症合并双眼视网膜病变一例[J].中华眼底病杂志,2005,21(6):402-402. 被引量:7
  • 4刘瑛,李承新.色素失禁症1例[J].中国皮肤性病学杂志,2006,20(1):47-48. 被引量:4
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  • 10Aradhya S, Woffendin H, Jakins T, et al. A recurrent deletion in the ubiquitously expressed NEMO (IKK-gamma) gene accounts for the vast majority of incontinentia pigmenti mutations [J]. Hum MolGenet, 2001, 10(19):2171-2179.

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