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Published in: Journal of Inherited Metabolic Disease 6/2010

Open Access 01-12-2010 | Original Article

Neurocognitive functioning in school-aged cystinosis patients

Authors: M. T. P. Besouw, G. M. Hulstijn-Dirkmaat, R. E. A. van der Rijken, E. A. M. Cornelissen, C. M. van Dael, J. Vande Walle, M. R. Lilien, E. N. Levtchenko

Published in: Journal of Inherited Metabolic Disease | Issue 6/2010

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Abstract

Introduction

Cystinosis is an autosomal recessive disorder leading to intralysosomal cystine accumulation in various tissues. It causes renal Fanconi syndrome and end stage renal failure around the age of 10 years if not treated with cysteamine. Children with cystinosis seem to have a normal intelligence but frequently show learning difficulties. These problems may be due to specific neurocognitive deficits rather than impaired renal function. Whether cysteamine treatment can improve cognitive functioning of cystinosis patients is thus far unknown. We aim to analyze neurocognitive functioning of school-aged cystinosis patients treated with cysteamine in order to identify specific deficits that can lead to learning difficulties.

Patients and methods

Fourteen Dutch and Belgian school-aged cystinosis patients were included. Glomerular filtration rate was estimated using the Schwartz formula. Children were tested for general intelligence, visual-motor integration, inhibition, interference, sustained attention, accuracy, planning, visual memory, processing speed, motor planning, fluency and speed, and behavioural and emotional functioning using standardized methods.

Results

Glomerular filtration rate ranged from 22 to 120 ml min−1 1.73 m−2. Median full-scale intelligence was below the average of a normal population (87, range 60–132), with a discrepancy between verbal (median 95, range 60–125) and performance (median 87, range 65–130) intelligence. Over 50% of the patients scored poorly on visual-motor integration, sustained attention, visual memory, planning, or motor speed. The other tested areas showed no differences between patients’ and normal values.

Conclusion

Neurocognitive diagnostics are indicated in cystinosis patients. Early recognition of specific deficits and supervision from special education services might reduce learning difficulties and improve school careers.
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Metadata
Title
Neurocognitive functioning in school-aged cystinosis patients
Authors
M. T. P. Besouw
G. M. Hulstijn-Dirkmaat
R. E. A. van der Rijken
E. A. M. Cornelissen
C. M. van Dael
J. Vande Walle
M. R. Lilien
E. N. Levtchenko
Publication date
01-12-2010
Publisher
Springer Netherlands
Published in
Journal of Inherited Metabolic Disease / Issue 6/2010
Print ISSN: 0141-8955
Electronic ISSN: 1573-2665
DOI
https://doi.org/10.1007/s10545-010-9182-7

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