WAGRO syndrome: a rare genetic condition associated with aniridia and additional ophthalmologic abnormalities

Maria Angélica Tosi Ferreira¹; Ivan Gonçalves de Almeida Júnior¹; Daniel Kanami Kuratani¹; Rafael Fabiano Machado Rosa^1,2; João Francisco de Oliveira Gonzales¹; Lisieux Elaine de Borba Telles³; Ygor Arzeno Ferrão⁴; Paulo Ricardo Gazzola Zen^1,2

DOI: 10.5935/0004-2749.20190065

1. Universidade Federal de Ciências da Saúde de Porto Alegre, Porto Alegre, RS, Brazil
2. Clinical Genetics, Santa Casa de Misericórdia de Porto Alegre, Porto Alegre, RS, Brazil
3. Department of Psychiatry, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil
4. Department of Psychiatry, Universidade Federal de Ciências da Saúde de Porto Alegre, Porto Alegre, RS, Brazil

Corresponding author

Paulo Ricardo Gazzola Zen
Genética Clínica - UFCSPA/SCMCPA
Rua Sarmento Leite, 245/403
Porto Alegre - RS - 90050-170 - Brazil
E-mail: [email protected]

Funding: No specific financial support was available for this study.

Disclosure of potential conflicts of interest: None of the authors have any potential conflicts of interest to disclose.

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How to cite this article:

Ferreira MAT, Almeida Júnior IG, Kuratani DK, Rosa^{1 RFM, 2} , Gonzales JFO, et al. Síndrome WAGRO: uma condição genética rara associada à aniridia e a anormalidades oftalmológicas adicionais. Arq. Bras. Oftalmol. 2019;82(4):. 10.5935/0004-2749.20190065

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