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[Vogt-Koyanagi-Harada syndrome: a serious and rare emergency in children].

作者信息

Venaille A, Palombi K, Templier I, Bouillet L, Pagnier A, Debillon T, Bourdat-Michel G

机构信息

Clinique universitaire de pédiatrie, CHU de Grenoble, Grenoble cedex 09, France.

出版信息

Arch Pediatr. 2011 Jan;18(1):33-6. doi: 10.1016/j.arcped.2010.09.013. Epub 2010 Nov 4.

DOI:10.1016/j.arcped.2010.09.013
PMID:21055910
Abstract

Uveitis in children is a rare disease, often going undiagnosed. Vogt-Koyanagi-Harada syndrome, a uveomeningeal disease from an autoimmune process, rarely affects children, but an early diagnosis is essential in order to begin systemic corticosteroid therapy within the shortest delay possible for a better visual prognosis. We report a case of a 10-year-old boy, already treated with corticosteroids for the last 3 years for a nephrotic syndrome, referred for a sudden decrease in visual acuity affecting both eyes, associated with typical cutaneous manifestations of the disease.

摘要

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