Klin Monbl Augenheilkd 2011; 228(4): 368-371
DOI: 10.1055/s-0031-1273265
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© Georg Thieme Verlag KG Stuttgart · New York

Vogt-Koyanagi-Harada Syndrome Manifestations and Diagnosis

Manifestationen und Diagnostik des Vogt-Koyanagi-Harada-SyndromsJ. M. Katsimpris, P. E. Theoulakis, J. Lepidas, A. Livieratou, I. K. Petropoulos
Further Information

Publication History





Publication Date:
11 April 2011 (online)

Introduction

Vogt-Koyanagi-Harada (VKH) syndrome is a rare multisystemic idiopathic disorder that affects tissues with melanocytes. The exact cause remains unknown. It is a diffuse bilateral granulomatous panuveitis that is frequently accompanied by neurological, auditory and dermatological alterations [1]. The diagnosis is a challenge because of the rarity of VKH syndrome and it is based mainly on clinical criteria, with supportive evidence from ancillary tests. We hereby report two VKH syndrome cases, diagnosed and successfully treated.

References

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John M. Katsimpris MD, PhD

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