Cranial Arteriopathy in Familial Vogt-KoyanagiHarada Syndrome

Stephen J. Ryan; L. Creed Pettigrew

doi:10.1111/jon199554244

Cranial Arteriopathy in Familial Vogt-KoyanagiHarada Syndrome

Stephen J. Ryan, L. Creed Pettigrew

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5 Scopus citations

Abstract

A 59-year-old woman with Vogt-KoyanagiHarada (VKH) syndrome presented with transient ischemic attacks. Magnetic resonance angiography showed multiple areas of stenosis affecting the intracranial portions of both internal carotid arteries. Conventional angiography confirmed these abnormalities and also demonstrated tapering stenosis of the extracran1al segment of the left internal carotid artery. This patient and her similarly affected daughter represent the first reported association between cranial arteriopathy and intergenerational passage of VKH syndrome.

Original language	English
Pages (from-to)	244-245
Number of pages	2
Journal	Journal of Neuroimaging
Volume	5
Issue number	4
DOIs	https://doi.org/10.1111/jon199554244
State	Published - 1995

Bibliographical note

Publisher Copyright:
© American Society of Neuroimaging.

ASJC Scopus subject areas

Radiology Nuclear Medicine and imaging
Clinical Neurology

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abstract = "A 59-year-old woman with Vogt-KoyanagiHarada (VKH) syndrome presented with transient ischemic attacks. Magnetic resonance angiography showed multiple areas of stenosis affecting the intracranial portions of both internal carotid arteries. Conventional angiography confirmed these abnormalities and also demonstrated tapering stenosis of the extracran1al segment of the left internal carotid artery. This patient and her similarly affected daughter represent the first reported association between cranial arteriopathy and intergenerational passage of VKH syndrome.",

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AB - A 59-year-old woman with Vogt-KoyanagiHarada (VKH) syndrome presented with transient ischemic attacks. Magnetic resonance angiography showed multiple areas of stenosis affecting the intracranial portions of both internal carotid arteries. Conventional angiography confirmed these abnormalities and also demonstrated tapering stenosis of the extracran1al segment of the left internal carotid artery. This patient and her similarly affected daughter represent the first reported association between cranial arteriopathy and intergenerational passage of VKH syndrome.

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Cranial Arteriopathy in Familial Vogt-KoyanagiHarada Syndrome

Abstract

Bibliographical note

ASJC Scopus subject areas

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