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Síndrome de Vogt-Koyanagi-Harada incompleta associada a HLA DRB1*01 em criança de quatro anos de idade: relato de caso Incomplete Vogt-Koyanagi-Harada syndrome associated with HLA DRB1*01 in a 4-year-old child: case report

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  • معلومة اضافية
    • بيانات النشر:
      Conselho Brasileiro de Oftalmologia, 2007.
    • الموضوع:
      2007
    • نبذة مختصرة :
      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.
    • ISSN:
      1678-2925
      0004-2749
    • Rights:
      OPEN
    • الرقم المعرف:
      edsair.doajarticles..ad8032d8e675975ebb2f063d40ced7c3