莫比乌斯综合征:文献综述。

Child neurology open Pub Date : 2023-10-18 eCollection Date: 2023-01-01 DOI:10.1177/2329048X231205405
Syed Abdullah Monawwer, Sajjad Ali, Raahim Naeem, Syed Hasan Ali, Azkah Rabbani, Maria Khan, Saba Saleem Qazi, Syed Muhammad Ismail Shah, Sabeeh Khawar Farooqui
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引用次数: 0

摘要

Moebius综合征是一种罕见的非进行性先天性神经病理学综合征,主要以面部(CN VII)和外展神经(CN VI)发育不全为特征。Moebius综合征的其他特征包括面神经麻痹、眼肌麻痹、正畸缺陷(包括牙列拥挤、牙龈肿胀和增生、牙石等)、肌肉骨骼异常和精神功能受损。由于这种疾病的罕见性,文献中很少报道病例研究。本文根据报告病例的共性总结了该疾病的显著特征,以及最近文献中引用的几个新认识的特征。我们已经探索了不同的诊断标准和可能使用的新识别的成像模式。可以理解的是,这种情况会对患者的生活质量产生不利影响;因此,还概述了治疗措施。本研究旨在提供关于Moebius综合征MBS的最新文献,并提高对该疾病的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Moebius Syndrome: An Updated Review of Literature.

Moebius Syndrome, is a rare, non-progressive congenital neuropathological syndrome characterized primarily by the underdevelopment of the facial (CN VII) and abducens nerve (CN VI). Other features of Moebius Syndrome include facial nerve paresis, ophthalmoplegias, orthodontic deficiencies (including crowded dentition, swollen and hyperplastic gingiva, dental calculus, etc.), musculoskeletal abnormalities, and impaired mental function. Due to the rarity of the disorder, very few case studies have been reported in the literature. This article summarizes the significant features of the disease according to commonalities in reported cases, along with several newly recognized features cited in recent literature. We have explored the different diagnostic criteria and the newly recognized imaging modalities that may be used. Understandably, the condition detrimentally affects a patient's quality of life; thus, treatment measures have also been outlined. This study aims to provide updated literature on Moebius Syndrome MBS and improve understanding of the condition.

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