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

Ezgi Karataş¹; Canan Aslı Utine^2,3,4

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: cananutine@gmail.com

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How to cite this article:

Karataş E, Utine^{2 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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