Fels Rebecca
From the Clinical Vision Science Faculty of Health, IWK Health Centre Eye Clinic, Dalhousie University, Halifax, Nova Scotia, Canada.
Am Orthopt J. 2017 Jan;67(1):89-92. doi: 10.3368/aoj.67.1.89.
Congenital cranial dysinnervation disorders (CCDD) is a new term describing a collection of non-progressive neurogenic syndromes. Initially referred to as congenital fibrosis syndrome, it was thought that the primary problem was extraocular muscular maldevelopment. Recent advancements in genetics and neuro-radiology have now determined the initial observation of fibrotic muscles is secondary to a primary lack of innervation from deficient, absent, or misguided cranial nerves. This presentation provides an overview of the known genes and phenotypes currently recognized within the CCDD domain. It will also highlight areas of current research being done in the area of cranial nerve development. Increased knowledge and awareness of these disorders has resulted in more research being conducted. These studies have provided a more complete understanding of efferent motor system development and are leading to improved treatment strategies for patients.
先天性颅神经支配障碍(CCDD)是一个描述一组非进行性神经源性综合征的新术语。最初被称为先天性纤维化综合征,人们认为主要问题是眼外肌发育不良。遗传学和神经放射学的最新进展现已确定,最初观察到的纤维化肌肉是由于颅神经缺乏、缺失或走行异常导致的原发性神经支配不足所致。本报告概述了目前在CCDD领域中已知的基因和表型。它还将突出当前在颅神经发育领域正在进行研究的领域。对这些疾病的更多了解和认识导致了更多的研究开展。这些研究对传出运动系统的发育有了更全面的理解,并正在为患者带来更好的治疗策略。