Reiss A L, Freund L, Tseng J E, Joshi P K
Behavioral Genetics Research Center, Johns Hopkins University School of Medicine, Baltimore, MD 21205.
Am J Hum Genet. 1991 Aug;49(2):279-88.
The relative homogeneity of the neuropsychiatric phenotype in individuals with fragile (fra) X syndrome suggests that there are consistent central nervous system (CNS) abnormalities underlying the observed cognitive and behavioral abnormalities. In this study, the neuroanatomy of the posterior fossa and other selected CNS regions in 12 young fra X females were compared with those of a group of 12 age-, sex-, and IQ-matched females without evidence of the fra X syndrome. Fra X females were shown to have decreased size of the posterior cerebellar vermis and increased size of the fourth ventricle, findings that are identical to those previously reported for fra X males. When compared with fra X male and nonfra X control groups, the distribution of the posterior-vermis and fourth-ventricle variables for the fra X female group was intermediate. These results support the hypothesis that the fra X genetic abnormality leads to hypoplasia of the posterior cerebellar vermis, a neuroanatomical variation of potential importance to both developmental and neuropsychiatric syndromes.
脆性X综合征患者神经精神表型的相对同质性表明,在观察到的认知和行为异常背后存在一致的中枢神经系统(CNS)异常。在本研究中,将12名年轻脆性X综合征女性患者后颅窝及其他选定CNS区域的神经解剖结构与12名年龄、性别和智商匹配且无脆性X综合征迹象的女性进行了比较。结果显示,脆性X综合征女性患者小脑蚓部后部尺寸减小,第四脑室尺寸增大,这一结果与之前报道的脆性X综合征男性患者相同。与脆性X综合征男性和非脆性X综合征对照组相比,脆性X综合征女性组后蚓部和第四脑室变量的分布处于中间状态。这些结果支持了以下假说:脆性X基因异常导致小脑蚓部后部发育不全,这一神经解剖学变异对发育和神经精神综合征可能具有重要意义。