首页> 美国卫生研究院文献>other >Kaposi sarcoma oral malformations mitral dysplasia and scoliosis associated with 7q34-q36.3 heterozygous terminal deletion
【2h】

Kaposi sarcoma oral malformations mitral dysplasia and scoliosis associated with 7q34-q36.3 heterozygous terminal deletion

机译:卡波西氏肉瘤口腔畸形二尖瓣发育不良和脊柱侧弯与7q34-q36.3杂合末端缺失相关

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Chromosome 7 germline macrodeletions have been implicated in human congenital malformations and developmental delays. We herein report a novel heterozygous macrodeletion of 7q34-q36.3 in a 16-year-old girl originally from West Indies. Similar to previously reported cases of germline chromosome 7q terminal deletions, our patient has dental malposition, and developmental (growth and intellectual) delay. Novel phenotypic features include endemic Kaposi sarcoma, furrowed tongue, thoracolumbar scoliosis, and mild mitral valve dysplasia. The occurrence of human herpes virus 8-driven Kaposi sarcoma, in a child otherwise normally resistant to other infectious agents and without any other tumoral lesion, points to a very selective immunodeficiency. While defects in organogenesis have been described with such macrodeletions, this is the first report of immunodeficiency and cancer predisposition.
机译:染色体7种系的大缺失与人类先天性畸形和发育延迟有关。我们在本文中报道了最初来自西印度群岛的16岁女孩中7q34-q36.3的新型杂合性大缺失。与先前报道的种系染色体7q末端缺失类似,我们的患者出现牙齿错位以及发育(生长和智力)延迟。新的表型特征包括特有的卡波济肉瘤,皱巴巴的舌头,胸腰部脊柱侧弯和轻度二尖瓣发育不良。人疱疹病毒8驱动的卡波西肉瘤的发生,通常对其他传染病具有抵抗力,而没有任何其他肿瘤病变的儿童,则表明免疫选择性很强。虽然已经通过这种大缺失描述了器官发生中的缺陷,但这是免疫缺陷和癌症易感性的首次报道。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号