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Congenital hereditary endothelial dystrophy with progressive sensorineural deafness (Harboyan syndrome)
Harboyan syndrome is a degenerative corneal disorder defined as congenital hereditary endothelial dystrophy (CHED) accompanied by progressive, postlingual sensorineural hearing loss. To date, 24 cases from 11 families of various origin (Asian Indian, South American Indian, Sephardi Jewish, Brazilian...
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| Autors principals: | , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2008
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| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2576053/ https://ncbi.nlm.nih.gov/pubmed/18922146 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1750-1172-3-28 |
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