Grubben C, Fryns J P, De Zegher F, Van Den Berghe H
Centre for Human Genetics, University Hospital Leuven, Belgium.
Genet Couns. 1990;1(2):103-9.
Two cases of median cleft syndrome with associated basal encephalocele are presented. The median cleft face syndrome consists of several craniofacial defects and occurs, as far as we know, sporadically. Extracranial defects should be looked for carefully since they may indicate the presence of a specific syndrome with its own prognosis and mode of inheritance. Basal encephaloceles are sometimes part of the syndrome and may cause serious, or even life-threatening, symptoms. With regard to the treatment of basal encephaloceles there still exists a lot of controversion, but most authors agree that it is better to postpone operation until after the age of three because mortality is lower then.
本文报告两例伴有基底脑膨出的正中裂综合征病例。正中裂面综合征由多种颅面缺陷组成,据我们所知,其发病具有散发性。应仔细检查颅外缺陷,因为它们可能提示存在具有特定预后和遗传方式的特定综合征。基底脑膨出有时是该综合征的一部分,可能导致严重甚至危及生命的症状。关于基底脑膨出的治疗,仍存在很多争议,但大多数作者认为最好将手术推迟到三岁以后,因为那时死亡率较低。