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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Detalles Bibliográficos
Autores principales: Desir, Julie, Abramowicz, Marc
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2576053/
https://www.ncbi.nlm.nih.gov/pubmed/18922146
http://dx.doi.org/10.1186/1750-1172-3-28

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2576053/
https://www.ncbi.nlm.nih.gov/pubmed/18922146
http://dx.doi.org/10.1186/1750-1172-3-28

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