Abstract
The present study evaluated the color vision of 44 patients with Duchenne muscular dystrophy (DMD) (mean age 14.8 years; SD 4.9) who were submitted to a battery of four different color tests: Cambridge Colour Test (CCT), Neitz Anomaloscope, Ishihara, and American Optical Hardy-Rand-Rittler (AO H-R-R). Patients were divided into two groups according to the region of deletion in the dystrophin gene: upstream of exon 30 (n = 12) and downstream of exon 30 (n = 32). The control group was composed of 70 age-matched healthy male subjects with no ophthalmological complaints. Of the patients with DMD, 47% (21/44) had a red-green color vision defect in the CCT, confirmed by the Neitz Anomaloscope with statistical agreement (P <10% for the normal male population (P
Cite
CITATION STYLE
Costa, M. F., Oliveira, A. G. F., Feitosa-Santana, C., Zatz, M., & Ventura, D. F. (2007). Red-green color vision impairment in Duchenne muscular dystrophy. American Journal of Human Genetics, 80(6), 1064–1075. https://doi.org/10.1086/518127
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