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Bol. Asoc. Méd. P. R ; 96(2): 84-90, Mar.-Apr. 2004.
Artículo en Inglés | LILACS | ID: lil-411070

RESUMEN

PURPOSE: To study color vision in patients with oculocutaneous albinism (OCA) METHODS: We evaluated color vision in 42 patients with OCA using the HRR color plates. Sixty seven percent of the patients had the Hermansky-Pudlak syndrome (HPS), diagnosed genetically or clinically. The remaining patients had unknown mutations leading to OCA. RESULTS: 47.6 of patients of OCA of all types included had a color vision defect. Of these, 55 were female and 45 were male patients. 50 of patients with the HPS (all types) had a color vision deficit. 42.9 of patients with OCA of unknown type had color weakness. 57.1 had normal color vision. CONCLUSIONS: Results suggest that many patients with OCA and the HPS have a mild red-green color perception deficiency that is not a sex linked trait. The prevalence of color vision deficits in our study population increased with decreasing visual acuity


Asunto(s)
Masculino , Femenino , Preescolar , Niño , Adolescente , Adulto , Persona de Mediana Edad , Humanos , Percepción de Color , Defectos de la Visión Cromática/etiología , Síndrome de Hermanski-Pudlak/complicaciones , Albinismo Oculocutáneo/clasificación , Albinismo Oculocutáneo/complicaciones , Albinismo Oculocutáneo/fisiopatología , Defectos de la Visión Cromática/epidemiología , Defectos de la Visión Cromática/genética , Heterogeneidad Genética , Genotipo , Incidencia , Fenotipo , Estudios Prospectivos , Percepción de Color/genética , Proteínas de la Membrana/genética , Proteínas Portadoras/genética , Síndrome de Hermanski-Pudlak/clasificación , Síndrome de Hermanski-Pudlak/genética , Síndrome de Hermanski-Pudlak/fisiopatología , Agudeza Visual
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