Dilts C V, Carey J C, Kircher J C, Hoffman R O, Creel D, Ward K, Clark E, Leonard C O
Department of Pediatrics, University of Utah School of Medicine. Salt Lake City, USA.
J Dev Behav Pediatr. 1996 Aug;17(4):229-39.
Twenty 6- to 17-year-old children with neurofibromatosis 1. (NF1) were compared to 20 age- and sex-matched siblings on a wide range of neuropsychological and behavioral dimensions. In familial cases, diagnostic status was confirmed by gene linkage with greater than 98% accuracy. Visual examinations that included assessments of visual evoked responses (VER) were performed on subjects with NF1. Forty-two percent of NF1 subjects had abnormal VER and underwent magnetic resonance imagery or computed tomography scans of the brain. On a variety of skills, subjects with NF1 performed more poorly than unaffected siblings. Children with NF1 were found to be less competent on measures of cognitive, language, and motor development, visual-spatial judgment, visual-motor integration, and academic achievement. Learning disabilities were common in children with NF1. Parents and teachers reported that NF1 subjects had internalizing problems and difficulty interacting with peers. A behavioral phenotype for NF1 and recommendations for preventative interventions are proposed.
对20名6至17岁的1型神经纤维瘤病(NF1)患儿与20名年龄和性别匹配的同胞在广泛的神经心理学和行为维度上进行了比较。在家族性病例中,通过基因连锁分析确诊,准确率超过98%。对患有NF1的受试者进行了包括视觉诱发电位(VER)评估在内的视力检查。42%的NF1受试者VER异常,并接受了脑部磁共振成像或计算机断层扫描。在各种技能方面,患有NF1的受试者表现比未受影响的同胞更差。研究发现,NF1患儿在认知、语言和运动发育、视觉空间判断、视觉运动整合和学业成绩等方面的能力较低。学习障碍在NF1患儿中很常见。家长和教师报告称,NF1受试者存在内化问题,且与同龄人互动困难。本文提出了NF1的行为表型及预防性干预建议。