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患有罗斯综合征和节后霍纳综合征患者的自主神经功能障碍部位。

Site of autonomic dysfunction in a patient with Ross' syndrome and postganglionic Horner's syndrome.

作者信息

Wolfe G I, Galetta S L, Teener J W, Katz J S, Bird S J

机构信息

Department of Neurology, University of Texas Southwestern Medical Center, Dallas 75235-8897, USA.

出版信息

Neurology. 1995 Nov;45(11):2094-6. doi: 10.1212/wnl.45.11.2094.

DOI:10.1212/wnl.45.11.2094
PMID:7501165
Abstract

Ross' syndrome is a rare peripheral nervous system disorder defined by Adie's tonic pupil, hyporeflexia, and segmental anhidrosis. Injury to postganglionic cholinergic fibers is believed to account for the tonic pupil and sweating disturbance. We report a 47-year-old man found to have Ross' syndrome in combination with a complete postganglionic Horner's syndrome. Pharmacologic and sudomotor tests in this unique patient provide further evidence that Ross' syndrome results from injury to sympathetic and parasympathetic ganglion cells or to their postganglionic projections.

摘要

罗斯综合征是一种罕见的周围神经系统疾病,其特征为阿狄瞳孔、反射减退和节段性无汗。节后胆碱能纤维损伤被认为是导致强直性瞳孔和出汗障碍的原因。我们报告一名47岁男性,被发现患有罗斯综合征并伴有完全性节后霍纳综合征。对这名独特患者进行的药理学和发汗试验进一步证明,罗斯综合征是由交感神经和副交感神经节细胞或其节后投射损伤所致。

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Site of autonomic dysfunction in a patient with Ross' syndrome and postganglionic Horner's syndrome.患有罗斯综合征和节后霍纳综合征患者的自主神经功能障碍部位。
Neurology. 1995 Nov;45(11):2094-6. doi: 10.1212/wnl.45.11.2094.
2
Ross syndrome plus: beyond horner, Holmes-Adie, and harlequin.罗斯综合征附加症:超越霍纳氏综合征、福尔摩斯-阿迪综合征和丑角综合征。
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Tonic pupil, areflexia, and segmental anhidrosis: two additional cases of Ross syndrome and review of the literature.强直性瞳孔、无反射及节段性无汗症:另外两例罗斯综合征病例及文献综述
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Isolated generalised anhidrosis induced by postganglionic sympathetic skin nerve fibre degeneration: an incomplete Ross syndrome?节后交感皮肤神经纤维变性引起的孤立性全身性无汗症:一种不完全性罗斯综合征?
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[Idiopathic segmental anhidrosis].[特发性节段性无汗症]
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Ross' syndrome (tonic pupil plus).
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