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Genetic, clinical and electrophysiological aspects of albinism are described. Emphasis is placed on electrophysiological features which help to distinguish albinism from other clinical conditions,… Continue Reading
Hunter syndrome or Type II mucopolysaccharidosis is a rare disorder of mucopolysaccharide metabolism. We report the cases of two brothers with Hunter syndrome with the previously undocumented ocular… Continue Reading
Details of 22 members from three generations of a family exhibiting systemic and ocular abnormalities are presented. The former include mild mental retardation and a high incidence of abortion or… Continue Reading
Hearing-impaired children use vision to compensate for impaired auditory information. This fact, and the relatively high incidence of visual defect among the deaf population, render regular visual… Continue Reading