Visual evoked potential (VEP) has been used as an alternative method to assess visual
acuity objectively, especially in non-verbal infants and adults with low intellectual abilities or …

Human perceptual development evolves in a stereotyped fashion, with initially limited
perceptual capabilities maturing over the months or years following the commencement of …

Objective Rett syndrome (RTT) is a neurodevelopmental disorder caused by mutation of the
X‐linked MECP2 gene and characterized by developmental regression during the first few …

Despite the heterogeneity of the umbrella term cerebral visual impairment (CVI) to denote
visual dysfunction in early childhood that results from a wide range of developmental …

CDKL5 deficiency disorder (CDD) is a neurodevelopmental disorder characterized by a
severe global developmental delay and early-onset seizures. Notably, patients show …

Abstract The Forkead Box G1 (FOXG1 in humans, Foxg1 in mice) gene encodes for a DNA-
binding transcription factor, essential for the development of the telencephalon in …

Visual experience is crucial for the development of neural processing. For example, alpha
activity development is a vision-dependent mechanism. Indeed, studies report no alpha …

Cerebral ischemia can occur at any stage in life, but clinical consequences greatly differ
depending on the developmental stage of the affected brain structures. Timing of the lesion …

Background Carotenoids are antioxidant pigments that deposit in human tissues (eg, skin,
macula, and brain) upon dietary consumption. The health implications of skin carotenoids …

Background Duplication and deletion of the chromosomal region 16p11. 2 cause a broad
range of impairments, including intellectual disability, language disorders, and sensory …