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Ophthalmic Genet ; 18(2): 87-91, 1997 Jun.
Article in English | MEDLINE | ID: mdl-9228245

ABSTRACT

We studied two siblings with the rare association of corneal dystrophy and perceptive deafness (Harboyan syndrome). To our knowledge, this is the third description of this hereditary disorder. The results of the clinical, genetic, audiometric, and ocular examination of the two siblings and the type of inheritance, which agree with the previous description of the syndrome, are reported. Various hereditary syndromes associated with corneal dystrophy are reviewed.


Subject(s)
Corneal Dystrophies, Hereditary/genetics , Corneal Dystrophies, Hereditary/pathology , Deafness/genetics , Deafness/pathology , Adult , Cornea/pathology , Corneal Dystrophies, Hereditary/complications , Deafness/complications , Eye Abnormalities/genetics , Eye Abnormalities/pathology , Family Health , Female , Hearing Tests , Humans , Male , Pedigree , Visual Acuity/genetics , Visual Acuity/physiology
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