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
Arq. bras. oftalmol
; Arq. bras. oftalmol;70(2): 340-342, mar.-abr. 2007. ilus
Article
in Pt
| LILACS
| ID: lil-453179
Responsible library:
BR1.1
RESUMO
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.
ABSTRACT
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.
Key words
Full text:
1
Collection:
01-internacional
Database:
LILACS
Main subject:
Uveomeningoencephalitic Syndrome
Type of study:
Diagnostic_studies
/
Risk_factors_studies
Limits:
Child, preschool
/
Humans
/
Male
Language:
Pt
Journal:
Arq. bras. oftalmol
Journal subject:
OFTALMOLOGIA
Year:
2007
Document type:
Article
Affiliation country:
Brazil
Country of publication:
Brazil