RT Journal Article
SR Electronic
T1 Abnormal cognitive function in treated congenital hypopituitarism
JF Archives of Disease in Childhood
JO Arch Dis Child
FD BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health
SP 827
OP 830
DO 10.1136/adc.2003.029116
VO 89
IS 9
A1 K Brown
A1 J Rodgers
A1 H Johnstone
A1 W Adams
A1 M Clarke
A1 M Gibson
A1 T Cheetham
YR 2004
UL http://adc.bmj.com/content/89/9/827.abstract
AB Aims: To assess cognitive function in school age children with congenital pituitary hormone deficiency (PHD). Methods: Ten children with PHD (aged 6.0–15.6 years, mean 11.5 years) and sibling controls (aged 8.7–14.9 years, mean 12.1 years) were assessed using the Wechsler Intelligence Scale for Children (WISC–III UK). Results: The patients’ full scale IQ scores were all below average (mean 75, 95% CI 70–80), but were not significantly different to those of sibling controls (mean 82, 95% CI 75–89). There was no difference in verbal IQ between patients and siblings, but performance IQ was significantly reduced (mean 75, 95% CI 68–82 in patients; mean 88, 95% CI 80–96 in sibling controls). The reduced performance IQ reflected a poorer performance in tasks assessing perceptual organisational skills. Conclusions: Data suggest that children with PHD have an IQ that is below average when compared to the population norm and a reduced performance IQ when compared to sibling controls. This may reflect abnormal brain development or could be linked to the impact of hypoglycaemia or low thyroxine concentrations in early life. This information is of value when counselling parents and planning a child’s care and education, although further, more extensive studies of patients and siblings are required.