Specific cognitive deficits in young children with cystinosis: evidence for an early effect of the cystinosin gene on neural function.
case_control · Level III
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- Record sourced from PubMed, PMID 17643777.
- Also identified by PMC identifier 2001176.
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Abstract
Infantile nephropathic cystinosis is associated with a specific cognitive deficit in visual spatial processing in older children and adults. The cause of this deficit is unknown. This study was designed to determine whether the cognitive deficit is present in young children with cystinosis, suggesting an early effect of the genetic disorder on brain development. Young children (n = 25; age, 3-8 years) with cystinosis and 25 matched control subjects underwent cognitive testing, including tests of intelligence, visual perceptual, visual spatial, and visual motor functions. Children with cystinosis performed significantly more poorly on tests of visual spatial and visual motor function than did control subjects. Visual perceptual abilities were equivalent in the 2 groups. The same pattern of visual spatial deficit is present in young children with cystinosis as has previously been demonstrated in older children and adults, which suggests that there may be an influence of the cystinosis gene on brain development, rather than an adverse effect of prolonged cystine accumulation in the brain during childhood.
Medical subject headings
- Amino Acid Transport Systems, Neutral
- Cognition Disorders
- Cystinosis
- Gene Expression Regulation, Developmental
- Perceptual Disorders