ACADEMIC-ACHIEVEMENT IN INDIVIDUALS WITH INFANTILE NEPHROPATHIC CYSTINOSIS

Citation
Ao. Ballantyne et al., ACADEMIC-ACHIEVEMENT IN INDIVIDUALS WITH INFANTILE NEPHROPATHIC CYSTINOSIS, American journal of medical genetics, 74(2), 1997, pp. 157-161
Citations number
21
Categorie Soggetti
Genetics & Heredity
ISSN journal
01487299
Volume
74
Issue
2
Year of publication
1997
Pages
157 - 161
Database
ISI
SICI code
0148-7299(1997)74:2<157:AIIWIN>2.0.ZU;2-9
Abstract
The present study examined academic skills in children and young adult s with infantile nephropathic cystinosis, Cystinosis is a genetic meta bolic disorder in which the amino acid cystine accumulates in various tissues and organs, including the kidney, cornea, thyroid, and brain, Individuals with cystinosis have normal intelligence but subtle visual processing impairments, Subjects were 19 children and young adults wi th cystinosis and 19 age-, sex-, and IQ-matched controls, All subjects had IQs within the normal range. On a test of academic achievement, m ean standard scores for cystinosis and control subjects, respectively, were as follows: arithmetic 89.95 +/- 13.77 vs. 102.16 +/- 9.62; spel ling 90.68 +/- 18.81 vs. 98.00 +/- 10.96; reading 97.47 +/- 15.59 vs, 98.58 +/- 12.41, Multivariate analysis of variance revealed a signific ant main effect for Group (P = .009); there was no main effect for Sex , nor was there a Group x Sex interaction. Univariate follow-up tests indicated that the cystinosis group performed significantly more poorl y than did controls on the arithmetic subtest (P = .001) and that ther e was a trend (P = .085) toward poorer performance by the cystinosis g roup on the spelling subtest. Regression analyses revealed no evidence of a developmental lag or deterioration of function with age, The vis ual processing deficits previously identified in these individuals may underlie the academic difficulties observed here, It is possible that both visual processing and academic difficulties may reflect a common mechanism of selective cortical damage by this genetic defect. (C) 19 97 Wiley-Liss, Inc.