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To the Editor: We read with a special interest the article by Helvestone and Gilmore [1] that described a case with uveitis, poliosis, and recurrent encephalomyelitis without meningitis diagnosed as a Vogt-Koyanagi-Harada syndrome (VKH). The patient had recurrent histories of remission and relapse with encephalomyelitis, there were periventricular and pontine hyperintense areas in T …
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