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1.
Clin Exp Rheumatol ; 42(7): 1507-1512, 2024 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-38819950

RESUMO

OBJECTIVES: To evaluate the effectiveness of the anterior segment optical coherence tomography (AS-OCT) for the screening of anterior uveitis in children diagnosed with juvenile idiopathic arthritis (JIA). METHODS: A cross-sectional, observational, non-randomised study was conducted in JIA patients younger than 18 years. All patients underwent anterior segment (AS-OCT) and macular OCT. RESULTS: A total of 300 eyes of 150 patients diagnosed with JIA were included; 74% were females, and mean age was 11.12 ± 3.51 years old (range 4.13-18.60). In the slit-lamp examination, anterior uveitis was diagnosed in 16 eyes. In the AS-OCT, anterior uveitis was suspected in 27 eyes; cells were detected in 27 eyes and retrokeratic precipitates in 5 eyes. Sensitivity was 0.94 and specificity was 0.96, positive predictive value was 0.59 and negative predictive value was 0.99, and Kappa-Cohen index was 0.71. CONCLUSIONS: AS-OCT could be considered for the screening of anterior segment uveitis in children diagnosed with JIA.


Assuntos
Artrite Juvenil , Tomografia de Coerência Óptica , Uveíte Anterior , Humanos , Artrite Juvenil/diagnóstico por imagem , Artrite Juvenil/complicações , Criança , Feminino , Masculino , Estudos Transversais , Adolescente , Uveíte Anterior/diagnóstico por imagem , Pré-Escolar , Valor Preditivo dos Testes , Câmara Anterior/diagnóstico por imagem , Câmara Anterior/patologia , Reprodutibilidade dos Testes
3.
Ophthalmic Genet ; 41(6): 656-658, 2020 12.
Artigo em Inglês | MEDLINE | ID: mdl-32940098

RESUMO

INTRODUCTION: Recently, You, Hoover-Fong, and colleagues described a disease caused by a deficiency of the telomere maintenance 2 gene (TELO2) function. The clinical spectrum includes early-onset global delay, dysmorphic facial features, auditory disorder, and reduced vision. MATERIALS AND METHODS: We report two siblings, diagnosed with You-Hoover-Fong syndrome at the age of 28 and 14 months. Both were genetically studied to find the cause of their developmental delay and microcephaly. RESULTS: The identical compound heterozygous missense mutations in the TELO2gene were found in each. Ophthalmologically, both siblings were diagnosed with progressive congenital bilateral nuclear-lamellar cataracts. CONCLUSIONS: We report nuclear-lamellar cataracts in two siblings diagnosed with You-Hoover-Fong syndrome.


Assuntos
Catarata/patologia , Deficiências do Desenvolvimento/patologia , Deficiência Intelectual/patologia , Microcefalia/patologia , Mutação de Sentido Incorreto , Homeostase do Telômero , Proteínas de Ligação a Telômeros/deficiência , Catarata/etiologia , Pré-Escolar , Deficiências do Desenvolvimento/complicações , Deficiências do Desenvolvimento/genética , Feminino , Humanos , Lactente , Deficiência Intelectual/complicações , Deficiência Intelectual/genética , Masculino , Microcefalia/complicações , Microcefalia/genética , Irmãos , Proteínas de Ligação a Telômeros/metabolismo
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