North K, Joy P, Yuille D, Cocks N, Hutchins P
Department of Neurology, Children's Hospital, Camperdown, Sydney, Australia.
Dev Med Child Neurol. 1995 May;37(5):427-36. doi: 10.1111/j.1469-8749.1995.tb12026.x.
The authors evaluated 51 consecutive children with NF1 (aged eight to 16 years) to determine the frequency of intelectual impairment and learning disability due to NF1 alone, the profile of learning disabilities and the effect of clinical variables. 40 children completed the full assessment protocol. There was no support for a profile of predominantly visuoperceptual deficits in the NF1 population. There was no discrepancy between verbal and performance IQ, and the deficits in function were wide ranging. Clinical variables such as age, sex, socio-economic status, disease severity, macrocephaly and family history of NF1 were not associated with cognitive deficits. These results emphasise the need for developmental evaluation to be included in the routine assessment of children with NF1.
作者评估了51名连续的1型神经纤维瘤病患儿(年龄8至16岁),以确定仅由1型神经纤维瘤病导致的智力障碍和学习障碍的发生率、学习障碍的特征以及临床变量的影响。40名儿童完成了完整的评估方案。没有证据支持1型神经纤维瘤病患者主要存在视觉感知缺陷的特征。言语智商和操作智商之间没有差异,功能缺陷范围广泛。年龄、性别、社会经济地位、疾病严重程度、巨头畸形和1型神经纤维瘤病家族史等临床变量与认知缺陷无关。这些结果强调了在1型神经纤维瘤病患儿的常规评估中纳入发育评估的必要性。