Advertisement

Article not rated

Vol. 6 - Num. 23

Clinical Reviews

Porphyries and colour blindness

Carmen Casaní Martíneza

aPediatra. Doctora en Medicina. CS de Burjassot (Valencia). Unidad de Neonatología, Hospital Universitario La Fe. Valencia. España.

Correspondence: C Casaní. E-mail: camarcar@alumni.uv.es

Reference of this article: Casaní Martínez C. Porphyries and colour blindness. Rev Pediatr Aten Primaria. 2004;6:415-419.

Published in Internet: 30-09-2004 - Visits: 8094

Abstract

Porphyries make a group of hereditary diseases caused by a partial defect in one of the seven enzymes of hem synthesis that generates a characteristic standard of accumulation and excretion of the correspondent precursor. Porphyries prevalence is 1/30000 in general population. Normal colour vision is called trichromasia because it is able to appreciate colour mixtures made with the three basic colours. 8% of men and 1% of women suffer from colour vision defects. A family in which both pathologies coincide is presented: the father suffers from a porphyria cutanea tarda, the youngest brother has a colour vision defect and the eldest brother both pathologies.

Keywords

Colour blindness Colour vision defect Porphyria Porphyria cutanea tarda

This content is not available in html format but you may download it in Acrobat Reader (PDF).

Comments

This article has no comments yet.