Vitamin A supplements for young children aged 6–59 months The World Health Organization (WHO) recommends that all children aged 6–59 months should receive supplements if they live in a community where VAD is a public health problem. These are communities where the prevalence of night blindness is ≥ 1% in children aged 24–59 months, or where the prevalence of VAD is ≥ 20% in infants and children...

X linked congenital stationary night blindness (CSNBX) is a non-progressive retinal disorder characterised by decreased visual acuity and disturbance of night vision. CSNBX appears to be not only clinically but also genetically heterogeneous. On studying a single large family, we recently suggested the presence of a distinct locus for CSNBX in Xp21.1. Here, we describe the results of a linkage ...

Vitamin A has probably been known for at least 3500 years as a factor that can cure a deficiency disease. Ancient Egyptians appear to have recognized night blindness, which we now know to be caused by vitamin A deficiency, and found a cure for it (1). However, this view has been disputed by modern scholars (2): the papyrus Ebers (ca. 1500 B.C.) (1) mentions an unspecified eye disease, sharew, b...

PURPOSE Congenital stationary night blindness is a nonprogressive retinal disorder manifesting as impaired night vision and is generally associated with other ocular symptoms, such as nystagmus, myopia, and strabismus. This study was conducted to further investigate the genetic basis of CSNB in a consanguineous Pakistani family. METHODS A consanguineous family with multiple individuals manife...

This study determined the prevalence of ocular manifestation of vitamin A deficiency in Orang Asli (Aborigine) children. Night blindness was found in 16.0% of the children, conjunctiva xerosis in 57.3%, Bitot's spot in 2.8%, corneal xerosis in 0.5% and corneal scars in 5.6%. These findings show that history of night blindness had sensitivity, specificity and predictive value (positive) of 47.2,...

A five generation family with an X linked ocular disorder has been investigated. The major clinical features were reduced visual acuity, nystagmus, and myopia. Although impaired night vision was not a symptom, using psychophysical and electrophysiological testing both rod and cone function were found to be abnormal in all affected males. No abnormality was detected in carrier females. Gene loca...