SciELO - Scientific Electronic Library Online

 
vol.17 issue2Personalization of the intraocular lens calculation formulasResults of phacoemulsification in 4 years of experience author indexsubject indexarticles search
Home Pagealphabetic serial listing  

Services on Demand

Article

Indicators

  • Have no cited articlesCited by SciELO

Related links

  • Have no similar articlesSimilars in SciELO

Share


Revista Cubana de Oftalmología

On-line version ISSN 1561-3070

Abstract

TABOADA LUGO, Noel; LARDOEYT FERRER, Roberto  and  RANGEL FLEITES, Rubén. Dominant autosomal hereditary optical atrophy: Apropos of a family. Rev Cubana Oftalmol [online]. 2004, vol.17, n.2, pp. 0-0. ISSN 1561-3070.

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.

Keywords : Optical atrophy [inheritance]; optical atrophy [simple or monosymptomatic].

        · abstract in Spanish     · text in Spanish

 

Creative Commons License All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License