Exfoliation syndrome associated with LOXL1 gene polymorphisms in a Black patient from Latin America: a case report

Guilherme Eiichi da Silva Takitani; Alexandre Gomes Bortoloti de Azevedo; Fabiana Louise Motta; Sérgio Henrique Teixeira; Juliana Maria Ferraz Sallum; Roberto Murad Vessani

DOI: 10.5935/0004-2749.20180084

Department of Ophthalmology, Universidade Federal de São Paulo, São Paulo, SP, Brazil

Corresponding author

Guilherme Eiichi da Silva Takitani
Departamento de Oftalmologia da EPM-UNIFESP
Rua Botucatu, 821
São Paulo, SP - 04023-062 - 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:

Takitani GES, Azevedo AGB, Motta FL, Teixeira SH, Sallum JMF, Vessani RM. Síndrome de esfoliação associada a polimorfismos do gene LOXL1 em paciente negro da América Latina: relato de caso. Arq. Bras. Oftalmol. 2018;81(5):. 10.5935/0004-2749.20180084

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