首页> 外文期刊>European journal of paediatric neurology: EJPN : official journal of the European Paediatric Neurology Society >Congenital Harlequin syndrome as an isolated phenomenon: A case report and review of the literature
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Congenital Harlequin syndrome as an isolated phenomenon: A case report and review of the literature

机译:先天性丑角综合征为孤立现象:一例病例报告并文献复习

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摘要

Harlequin syndrome (HS) is a rare autonomic disorder due to a hemifacial cutaneous sympathetic denervation. It is characterized by unilateral diminished sweating and flushing of the face even though after heat or prolonged exercise. It is typically acquired. Congenital cases only represent a 6% of all individuals with HS. All congenital HS cases reported so far showed a concomitant Homer syndrome, probably due to a stellate ganglion involvement. HS represents an uncommon autonomic disorder due to a hemifacial cutaneous sympathetic denervation. It is clinically characterized by a dramatic alteration in facial appearance: ipsilateral denervated pale and dry half from the other intact red and moist half. Conclusion: We present, to the best of our knowledge, the first case of a patient with a congenital HS as an isolated phenomenon. (C) 2016 European Paediatric Neurology Society. Published by Elsevier Ltd. All rights reserved.
机译:丑角综合症(HS)是一种罕见的植物神经失调症,由于半面部皮肤交感神经支配。它的特点是即使加热或长时间运动后,单侧汗液和脸红也会减少。通常是获取的。先天性病例仅占所有HS患者的6%。迄今为止,所有报告的先天性HS病例均显示并发荷马综合征,这可能是由于星状神经节受累所致。由于半面部皮肤交感神经失调,HS代表一种罕见的自主神经疾病。它的临床特征是面部外观发生巨大变化:同侧神经从另一完整无损的红色和湿润的一半去掉了苍白干燥的一半。结论:就我们所知,我们介绍了第一例先天性HS患者为孤立现象。 (C)2016欧洲儿科神经病学会。由Elsevier Ltd.出版。保留所有权利。

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