首页> 外文期刊>International journal of pediatric otorhinolaryngology >Otofaciocervical syndrome and metachondromatosis in a girl: Presentation of a novel association and remarks on clinical variability of branchial-arch disorders
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Otofaciocervical syndrome and metachondromatosis in a girl: Presentation of a novel association and remarks on clinical variability of branchial-arch disorders

机译:一名女孩的耳面颈部综合征和软骨软骨病:一种新颖的结合表现和有关arch弓畸形临床变异性的评论

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摘要

Otofaciocervical syndrome (OFCS) is a rare disorder characterized by facial, ear, branchial, and musculoskeletal anomalies, along with hearing loss and mild intellectual disability. Clinically, its distinction from branchiootorenal syndrome can be difficult. To date, the coexistence of OFCS and metachondromatosis has not been reported. Here, we describe a sporadic patient with both OFCS and metachondromatosis. This novel association prompts us to do some remarks on the clinical variability of branchial-arch disorders; in fact, our observations are consistent with the highly variable expressivity of OFCS and illustrate the need of a more accurate characterization of these branchial-arch disorders. In the meantime, involvement of clavicles, scapulae and shoulders remains a distinctive feature of OFCS. (C) 2016 Elsevier Ireland Ltd. All rights reserved.
机译:耳面宫颈综合征(OFCS)是一种罕见的疾病,其特征是面部,耳部,分支和肌肉骨骼异常,以及听力下降和轻度智力障碍。在临床上,将其与支气管肾综合征相区别可能很困难。迄今为止,还没有报道OFCS和软骨病共存。在这里,我们描述了一个既有OFCS又有软骨病的散发患者。这种新颖的联系促使我们对branch弓畸形的临床变异性做一些评论。实际上,我们的观察结果与OFCS的高度可变表达相吻合,并说明了需要对这些branch门畸形进行更准确表征的需求。同时,锁骨,肩骨和肩膀的受累仍然是OFCS的一个独特特征。 (C)2016 Elsevier Ireland Ltd.保留所有权利。

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