Vles J S, Fryns J P, Folmer K, Boon P, Buttiens M, Grubben C, Janevski B
Department of Child Neurology, University of Maastricht, The Netherlands.
Genet Couns. 1990;1(2):97-102.
This report gives a description of 4 male patients, two of whom are sibs, two of whom are uncle and cousin. They appear to have psychomotor retardation, spastic quadriparesis and on CT (partial) agencies of the corpus callosum, and irregular lining of the lateral ventricles, without craniofacial abnormalities or seizures. Although the mode of inheritance of agenesis of the corpus callosum is still difficult to establish, in these 4 male patients an X-linked recessive inheritance is the most likely mode. A review of the literature with concern to the heredity of agenesis of the corpus callosum is presented. The clinical and neurological findings in the present four male patients allow for the delineation of a new X-linked mental retardation syndrome.
本报告描述了4名男性患者,其中两名是同胞兄弟,两名是叔侄关系。他们表现出精神运动发育迟缓、痉挛性四肢瘫痪,CT显示胼胝体部分发育不全,侧脑室壁不规则,无颅面异常或癫痫发作。尽管胼胝体发育不全的遗传模式仍难以确定,但在这4名男性患者中,X连锁隐性遗传是最可能的模式。本文对胼胝体发育不全的遗传相关文献进行了综述。目前这4名男性患者的临床和神经学表现有助于明确一种新的X连锁智力障碍综合征。