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Atrofia óptica hereditaria autosómica dominante: A propósito de una familia / Dominant autosomal hereditary optical atrophy: Apropos of a family
Taboada Lugo, Noel; Lardoeyt Ferrer, Roberto; Rangel Fleites, Rubén.
  • Taboada Lugo, Noel; Centro Provincial de Genética Villa Clara. Villa Clara. CU
  • Lardoeyt Ferrer, Roberto; Centro Provincial de Genética Villa Clara. Villa Clara. CU
  • Rangel Fleites, Rubén; Centro Provincial de Genética Villa Clara. Villa Clara. CU
Rev. cuba. oftalmol ; 17(2)jul.-dic. 2004. ilus, tab
Article in Spanish | LILACS | ID: lil-629436
RESUMEN
Entre las causas de pérdida insidiosa, bilateral y simétrica de la visión central se deben tener siempre presente las atrofias ópticas heredo degenerativas. La atrofia óptica hereditaria autosómica dominante es la forma más frecuente de atrofia óptica heredofamiliar simple o monosintomática. Se realizó la caracterización clínica de una familia con el diagnóstico de esta discapacidad visual.
ABSTRACT
Among the causes of insidious, bilateral and symmetric loss of the central vision, the hereditary and degenerative optical atrophies should always be taken into account. The dominant autosomal hereditary optical atrophy is the most frequent form of simple or monosymptomatic hereditary family optical atrophy. The clinical characterization of a family with the diagnosis of this visual impairment was made.

Full text: Available Index: LILACS (Americas) Language: Spanish Journal: Rev. cuba. oftalmol Journal subject: Ophthalmology Year: 2004 Type: Article Affiliation country: Cuba Institution/Affiliation country: Centro Provincial de Genética Villa Clara/CU

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Full text: Available Index: LILACS (Americas) Language: Spanish Journal: Rev. cuba. oftalmol Journal subject: Ophthalmology Year: 2004 Type: Article Affiliation country: Cuba Institution/Affiliation country: Centro Provincial de Genética Villa Clara/CU