Sztriha László, Johansen Johan G, Al-Gazali Lihadh I
Department of Paediatrics, Faculty of Medicine and Health Sciences, United Arab Emirates University, Al Ain.
J Child Neurol. 2005 Feb;20(2):170-2. doi: 10.1177/08830738050200021301.
A 1-year-old boy with extreme microcephaly and a complex brain malformation is reported. Magnetic resonance imaging revealed an abnormal gyral pattern with features of the agyria-pachygyria spectrum, partial agenesis of the corpus callosum, severely hypoplastic posterior cerebellar vermis, and an abnormal foliation pattern of the cerebellar hemispheres associated with a flat and wide isthmus and pons. Although this phenotype shares some features with malformations classified as microcephaly with a simplified gyral pattern, microlissencephaly, or lissencephaly with cerebellar hypoplasia, none of the several subgroups of these categories are identical to the cerebral dysgenesis found in this patient.
报道了一名患有极度小头畸形和复杂脑畸形的1岁男孩。磁共振成像显示出异常的脑回模式,具有无脑回-巨脑回谱系的特征、胼胝体部分发育不全、小脑后蚓部严重发育不良,以及小脑半球异常的小叶模式,伴有扁平且宽阔的峡部和脑桥。尽管这种表型与归类为具有简化脑回模式的小头畸形、微小脑回畸形或伴有小脑发育不全的无脑回畸形的一些特征相同,但这些类别中的几个亚组均与该患者所发现的脑发育异常不完全相同。