Horner syndrome associated with ipsilateral facial and extremity anhydrosis

被引：6

作者：

Galvez, Alberto ^{[1
]}

Ailouti, Nadim ^{[2
]}

Toll, Agusti ^{[4
]}

Maria Espadaler, Josep ^{[2
]}

Roquer, Jaume ^{[3
]}

机构：

[1] Hosp del Mar, Serv Neurol, Barcelona 08003, Spain

[2] Hosp del Mar, Dept Neurophysiol, Barcelona 08003, Spain

[3] Hosp del Mar, Dept Neurol, Barcelona 08003, Spain

[4] Hosp del Mar, Dept Dermatol, Barcelona 08003, Spain

来源：

JOURNAL OF NEURO-OPHTHALMOLOGY | 2008年 / 28卷 / 03期

关键词：

D O I：

10.1097/WNO.0b013e318183cce0

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

We report a patient with Homer syndrome together with anhidrosis affecting the ipsilateral face and extremities confirmed with starch-iodine and sympathetic skin response testing. No anatomic lesion was apparent. This is the first reported case in which Homer syndrome has been associated with such extensive hemibody sympathetic dysfunction in the absence of other neurologic findings. We propose a developmental disorder of neural crest migration as the cause.

引用

页码：178 / 181

页数：4

共 21 条

[1]

Abe M, 2006, PEDIATR DERMATOL, V23, P358

[2]

*AM AC OPHTH, 2006, BAS CLIN SCI COURS N

[3] Coexisting harlequin and Horner syndromes after high thoracic paravertebral anaesthesia [J].