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Arq. Bras. Oftalmol. 2021; 84 (4): 10.5935/0004-2749.20210064

Total: 2676

Unusual clinical phenotype of Stargardt disease

Pedro Molina-Solana1; María José Morillo-Sánchez1; Cristina Méndez-Vidal2,3; Manuel Ramos-Jiménez4; Borja Domínguez-Serrano1; Guillermo Antiñolo2,3; Enrique Rodríguez-de-la-Rúa-Franch1,5

DOI: 10.5935/0004-2749.20210064

1. Department of Ophthalmology, University Hospital Virgen Macarena, Seville, Spain
2. Department of Maternofetal Medicine, Genetics and Reproduction, Institute of Biomedicine of Seville, University Hospital Virgen del Rocío/CSIC/ University of Seville, Seville, Spain
3. Rare Diseases Networking Biomedical Research Centre (CIBERER), Seville, Spain
4. Department of Clinical Neurophysiology, University Hospital Virgen Macarena, Seville, Spain. 5. Retics Oftared, Institute Carlos III, Madrid, Spain

Corresponding author

Pedro Molina-Solana
E-mail: [email protected]

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

Informed consent was obtained from all patients included in this study (PI15_01648 and CTS1664).


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How to cite this article:

Molina-Solana P, Morillo-Sánchez MJ, Méndez-Vidal2 C, 3 , Ramos-Jiménez M, Domínguez-Serrano B, et al. Fenótipo clínico incomum da doença de Stargardt. Arq. Bras. Oftalmol. 2021;84(4):. 10.5935/0004-2749.20210064
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