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Arq. bras. oftalmol ; 70(2): 340-342, mar.-abr. 2007. ilus
Article in Portuguese | LILACS | ID: lil-453179

ABSTRACT

A síndrome de Vogt-Koyanagi-Harada é doença crônica, sistêmica e auto-imune, com manifestações oculares, nervosas, auditivas e tegumentares. Descrevemos aqui o caso de uma criança com início dos sintomas aos quatro anos e dois meses de idade, com positividade para o HLA DRB1*01.


Vogt-Koyanagi-Harada syndrome is chronic systemic autoimmune disease with ocular, nervous, auditory and tegumental manifestations. We report here the case of a child with onset of symptoms at four years and two months of age, with positive HLA DRB1*01.


Subject(s)
Humans , Male , Child, Preschool , Uveomeningoencephalitic Syndrome/diagnosis , Uveomeningoencephalitic Syndrome/immunology , Cyclosporine/therapeutic use , Fluorescein Angiography , Fundus Oculi , Histocompatibility Testing , HLA-DR Antigens/immunology , Immunosuppressive Agents/therapeutic use , Retinal Vasculitis/diagnosis , Retinal Vasculitis/immunology , Uveomeningoencephalitic Syndrome/drug therapy , Visual Acuity
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