首页> 美国卫生研究院文献>Orphanet Journal of Rare Diseases >Craniocervical junction malformation in a child with Oromandibular-limb hypogenesis-Möbius syndrome
【2h】

Craniocervical junction malformation in a child with Oromandibular-limb hypogenesis-Möbius syndrome

机译:患有颌下肢发育不全-莫比乌斯综合征的儿童的颅颈交界畸形

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

We report a male child with Oromandibular-limb hypogenesis (OMLH), the main features being bilateral sixth and seventh nerve palsies, limb anomalies and hypoplasia of the tongue. Additional features were shortness of the neck associated with torticollis. Radiographs of the cervical spine were non-contributory, but 3D computed tomography (CT) scanning of this area identified: a) congenital hypoplasia of the atlas; b) the simultaneous development of occiput-atlas malformation/developmental defect. To our knowledge, this is the first clinical report assessing the cervico-cranium malformation in a child with OMLH-Möbius syndrome.
机译:我们报道了一名患有颌下肢发育不全(OMLH)的男孩,其主要特征是双侧第六和第七神经麻痹,肢体异常和舌头发育不全。其他特征是与斜颈相关的脖子短小。颈椎X线片无贡献,但对该区域进行3D计算机断层扫描(CT)扫描可确定:a)先天性寰椎发育不全; b)同时发生枕骨畸形/发育缺陷。据我们所知,这是评估OMLH-Möbius综合征患儿宫颈颅骨畸形的第一份临床报告。

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