File:Eye phenotype, untreated adult with Harboyan syndrome.jpg
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English: Eye phenotype, untreated adult with Harboyan syndrome. The cornea presents congenitally with a ground glass, bluish-white opaque cornea from diffuse edema of the stroma (1A). Slit lamp examination showing milkiness and increased thickness of the corneal (1B). Desir and Abramowicz Orphanet Journal of Rare Diseases 2008 3:28 doi:10.1186/1750-1172-3-28. The syndrome is called Autosomal recessive corneal dystrophy and perceptive deafness; CDPD; OMIM 217400 Русский: Дистрофия роговицы глаз при синдроме Харбояна (синдром, характеризующийся аутосомно-рецессивной дистрофией роговицы и перцептивной глухотой ) |
| Date | |
| Source | Congenital hereditary endothelial dystrophy with progressive sensorineural deafness (Harboyan syndrome) |
| Author | Julie Desir and Marc Abramowicz |
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© 2008 Desir and Abramowicz; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
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| current | 08:31, 5 August 2009 | | 1,200 × 352 (65 KB) | CopperKettle (talk | contribs) | {{Information |Description={{en|1=Eye phenotype, untreated adult with Harboyan syndrome. The cornea presents congenitally with a ground glass, bluish-white opaque cornea from diffuse edema of the stroma (1A). Slit lamp examination showing milkiness and in |
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