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Fabrice C. Deprez,Julie Coulier,Denis Rommel,Antonella Boschi 대한신경과학회 2015 Journal of Clinical Neurology Vol.11 No.2
Background Horner syndrome (HS), also known as Claude-Bernard-Horner syndrome oroculosympathetic palsy, comprises ipsilateral ptosis, miosis, and facial anhidrosis. Case Report We report herein the case of a 67-year-old man who presented with congenital HS associated with ipsilateral hypoplasia of the internal carotid artery (ICA), as revealedby heterochromia iridis and confrmed by computed tomography (CT). Conclusions CT evaluation of the skull base is essential to establish this diagnosis and distinguish aplasia from agenesis/hypoplasia (by the absence or hypoplasia of the carotid canal) orfrom acquired ICA obstruction as demonstrated by angiographic CT.