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Query: UMLS:C0029713 (immaturity)
 4,335 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

This is a targeted review of the critical immaturities limiting psychophysical luminance contrast detection in human infants. Three-month-old infants are 50 times less sensitive to contrast than adults are. Rod experiments suggest that early-stage immaturities, like the short length of infant rod outer segments, have only a modest direct effect on infant visual performance. Infant contrast sensitivity may resemble adult extrafoveal sensitivity, because the foveal cones of the neonate are immature and may not generate strong enough responses to mediate visual performance. This use of the extrafoveal retina reduces the high-spatial frequency end of the infant contrast sensitivity function (CSF), contributing to poor infant resolution acuity. The remaining difference between infant and adult CSFs may be a simple overall reduction in infant sensitivity. The maximum of the infant CSF increases proportionately with age, and may be numerically near the infant's age in weeks. Contrast discrimination experiments indicate that the critical immaturity that limits infant contrast sensitivity is a mid-level phenomenon, occurring before the site of the contrast gain control. For example, the infant ascending visual pathway might be limited by large amounts of intrinsic noise. These results suggest that there is little effect of inattentiveness to the psychophysical task by ostensibly alert infant patients or subjects. The clinician or researcher can interpret behavioral measurements of infant visual performance with confidence.
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PMID:Contrast insensitivity: the critical immaturity in infant visual performance. 1948 10

Visual sensory impairments are common in Mental Deficiency (MD) and Autism Spectrum Disorder (ASD). These defects are linked to cerebral dysfunction in the visual cortical area characterized by the deregulation of axon growth/guidance and dendrite spine immaturity of neurons. However, visual perception had not been addressed, although the retina is part of the central nervous system with a common embryonic origin. Therefore, we investigated retinal perception, the first event of vision, in a murine model of MD with autistic features. We document that retinal function is altered in Fmr1 KO mice, a model of human Fragile X Syndrome. Indeed, In Fmr1 KO mice had a lower retinal function characterized by a decreased photoreceptors neuron response, due to a 40% decrease in Rhodopsin content and to Rod Outer Segment destabilization. In addition, we observed an alteration of the visual signal transmission between photoreceptors and the inner retina which could be attributed to deregulations of pre- and post- synaptic proteins resulting in retinal neurons synaptic destabilization and to retinal neurons immaturity. Thus, for the first time, we demonstrated that retinal perception is altered in a murine model of MD with autistic features and that there are strong similarities between cerebral and retinal cellular and molecular defects. Our results suggest that both visual perception and integration must be taken into account in assessing visual sensory impairments in MD and ASD.
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PMID:Visual sensorial impairments in neurodevelopmental disorders: evidence for a retinal phenotype in Fragile X Syndrome. 2515 86