Serial intelligence test scores in pediatric moyamoya disease

被引:60
作者
Imaizumi, C
Imaizumi, T
Osawa, M
Fukuyama, Y
Takeshita, M
机构
[1] Imaizumi Pediat Clin, Maebashi, Gumma 3710023, Japan
[2] Tokyo Womens Med Coll, Dept Pediat, Tokyo 162, Japan
[3] Tokyo Womens Med Coll, Dept Neurosurg, Tokyo 162, Japan
关键词
moyamoya disease; childhood; intelligence quotient; chronological change;
D O I
10.1055/s-2007-973508
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Serial intelligence tests in 38 patients with childhood moyamoya disease were evaluated. A total of 98 tests were administered. The IQ scores were classified into three categories: tests performed between the time of onset of symptoms and 5 years after the onset of symptoms (n = 44), tests performed 5-10 years after the onset of symptoms (n=32), and tests performed more than 10 years after the onset of symptoms (n=22). When more than one test was performed during each period, the mean of the IQ scores was used. The IQ tests were administered two or more times to 10 patients in the onset-5-years category, and 5 of them exhibited lower IQ scores on later tests. The IQ scores were significantly lower in the 5-10 years category and in the more than 10 years category (76.8 +/- 23.1 and 73.9 +/- 31.1, respectively) than in the onset-5-years category (92.9 +/- 22.7). The IQ scores for the 5-10 years category and the more than 10 years category did not differ significantly. The IQ in pediatric moyamoya disease begins to decrease after the onset of symptoms, but the decline eventually stabilizes more than 10 years after the onset of symptoms.
引用
收藏
页码:294 / 299
页数:6
相关论文
共 21 条
[1]   CLINICAL AND ANGIOGRAPHIC FOLLOW-UP OF CHILDHOOD-ONSET MOYAMOYA DISEASE [J].
EZURA, M ;
YOSHIMOTO, T ;
FUJIWARA, S ;
TAKAHASHI, A ;
SHIRANE, R ;
MIZOI, K .
CHILDS NERVOUS SYSTEM, 1995, 11 (10) :591-594
[2]   Current state of study on Moyamoya disease in Japan [J].
Fukui, M .
SURGICAL NEUROLOGY, 1997, 47 (02) :138-143
[3]   CLINICAL AND CEREBRAL ANGIOGRAPHIC EVOLUTIONS OF IDIOPATHIC PROGRESSIVE OCCLUSIVE DISEASE OF THE CIRCLE OF WILLIS (MOYAMOYA DISEASE) IN CHILDREN [J].
FUKUYAMA, Y ;
UMEZU, R .
BRAIN & DEVELOPMENT, 1985, 7 (01) :21-37
[4]  
Houkin Kiyohiro, 1996, Neurologia Medico-Chirurgica, V36, P783, DOI 10.2176/nmc.36.783
[5]   Long-term outcomes of pediatric moyamoya disease monitored to adulthood [J].
Imaizumi, T ;
Hayashi, K ;
Saito, K ;
Osawa, M ;
Fukuyama, Y .
PEDIATRIC NEUROLOGY, 1998, 18 (04) :321-325
[6]   Effects of surgical revascularization on outcome of patients with pediatric moyamoya disease [J].
Ishikawa, T ;
Houkin, K ;
Kamiyama, H ;
Abe, H .
STROKE, 1997, 28 (06) :1170-1173
[7]  
ITO M, 1995, SHONI NO NOSHINKEI, V20, P264
[8]  
KARASAWA J, 1977, Neurologia Medico-Chirurgica, V17, P29, DOI 10.2176/nmc.17pt1.29
[9]  
KARASAWA J, 1980, SURG NEUROL, V14, P444
[10]   TREATMENT OF MOYAMOYA DISEASE WITH STA-MCA ANASTOMOSIS [J].
KARASAWA, J ;
KIKUCHI, H ;
FURUSE, S ;
KAWAMURA, J ;
SAKAKI, T .
JOURNAL OF NEUROSURGERY, 1978, 49 (05) :679-688