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

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]


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