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Arq. Bras. Oftalmol. 2025; 88 (2): 10.5935/0004-2749.2023-0078

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Congenital hereditary endothelial dystrophy with progressive sensorineural deafness: a case report of Harboyan syndrome

Ezgi Karataş1; Canan Aslı Utine2,3,4

DOI: 10.5935/0004-2749.2023-0078

1. Department of Ophthalmology, İbrahim Çeçen University Faculty of Medicine, Ağrı, Turkey
2. Department of Ophthalmology, Dokuz Eylül University Faculty of Medicine, Izmir, Turkey
3. Izmir Biomedicine and Genome Center, Izmir, Turkey
4. Department of Ophthalmology, University of Naples Federico II, Naples, Italy

Corresponding author

Canan Asli Utine
E-mail: [email protected]

Funding: This study received no specific financial support.

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:

Karataş E, Utine2 CA, 3 , 4 . Congenital hereditary endothelial dystrophy with progressive sensorineural deafness: a case report of Harboyan syndrome. Arq. Bras. Oftalmol. 2025;88(2):. 10.5935/0004-2749.2023-0078
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