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A further observation of corneal dystrophy and perceptive deafness in two siblings.
Magli, A; Capasso, L; Foà, T; Maurino, V; Ventruto, V.
Afiliación
  • Magli A; Istituto di Oftalmologia, Università degli Studi di Napoli Federico II, Italy. magli@ds.unina.it
Ophthalmic Genet ; 18(2): 87-91, 1997 Jun.
Article en En | 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.
Asunto(s)
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Distrofias Hereditarias de la Córnea / Sordera Límite: Adult / Female / Humans / Male Idioma: En Revista: Ophthalmic Genet Asunto de la revista: GENETICA MEDICA / OFTALMOLOGIA Año: 1997 Tipo del documento: Article País de afiliación: Italia
Buscar en Google
Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Distrofias Hereditarias de la Córnea / Sordera Límite: Adult / Female / Humans / Male Idioma: En Revista: Ophthalmic Genet Asunto de la revista: GENETICA MEDICA / OFTALMOLOGIA Año: 1997 Tipo del documento: Article País de afiliación: Italia