Opening the Pandora Box of Retinal Dystrophies: Is it Malattia Leventinese?

Authors

  • Inês Ludovico Serviço de Oftalmologia, Unidade Local de Saúde de São José, Lisboa, Portugal https://orcid.org/0009-0009-2097-0999
  • Pedro Lopes Serviço de Oftalmologia, Unidade Local de Saúde de São José, Lisboa, Portugal
  • Maria Elisa Luís Serviço de Oftalmologia, Unidade Local de Saúde de São José, Lisboa, Portugal

DOI:

https://doi.org/10.48560/rspo.42426

Keywords:

Choroidal Neovascularization, Optic Disk Drusen, Retinal Dystrophies

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References

1. Zhang T, Xie X, Cao G, Jiang H, Wu S, Su Z, et al. Malattia leventinese/Doyne honeycomb retinal dystrophy in a Chinese family with mutation of the EFEMP1 gene. Retina. 2014;34(12):2462-71.

2. Querques G, Souied EH, Soubrane G, Coscas G. Multimodal morphological and functional characterization of Malattia Leventinese. Graefes Arch Clin Exp Ophthalmol. 2013;251(3):705-14.

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Published

2025-09-16

How to Cite

Ludovico, I., Lopes, P., & Luís, M. E. (2025). Opening the Pandora Box of Retinal Dystrophies: Is it Malattia Leventinese?. Revista Sociedade Portuguesa De Oftalmologia, 49(3), 259–260. https://doi.org/10.48560/rspo.42426

Issue

Vol. 49 No. 3 (2025)

Section

Shot Communications and Images in Ophthalmology

License

Copyright (c) 2025 Revista Sociedade Portuguesa de Oftalmologia

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