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Article

Congenital hereditary endothelial dystrophy with progressive sensorineural deafness (Harboyan syndrome)

15 Oct 2008

Abstract excerpt

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 Portuguese, Dutch, Gypsy, Moroccan, Dominican) have been reported. More than 50% of the reported cases have been...

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Share to Anion Transport Proteins
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Share to Corneal Dystrophies, Hereditary

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 18922146
DOI: 10.1186/1750-1172-3-28

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