Robin N H, Ko L M, Heeger S, Muise K L, Judge N, Bangert B A
Department of Genetics, Case Western Reserve University, School of Medicine, Cleveland, Ohio, USA.
Am J Med Genet. 1996 Dec 30;66(4):433-7. doi: 10.1002/(SICI)1096-8628(19961230)66:4<433::AID-AJMG9>3.0.CO;2-L.
Here we report on an infant of a diabetic mother (IDM) with midline interhemispheric "fusion" (MIF), or syntelencephaly. This is a rare anomaly characterized by segmental failure of cleavage of the cerebral hemispheres and other brain structures in the posterior frontal and parietal regions, with a normal interhemispheric fissure anterior and posterior to the "fused" region. While there is obvious overlap with holoprosencephaly (HPE), this condition differs from HPE in that the midline "fusion" in MIF is complete but segmental, while the structural brain anomalies seen in the HPE spectrum progress smoothly in severity in a posterior to anterior "fusion." However, while it is apparent that there are key distinctions between MIF and HPE, in all likelihood they arise from a similar pathogenetic mechanisms. We therefore suggest that MIF is a distinct variant of the HPE spectrum of midline brain anomalies. Given the known increased incidence of HPE in IDMs, MIF is likely a maternal diabetes-associated malformation.
在此,我们报告一例患有中线半球间“融合”(MIF)即并脑畸形的糖尿病母亲婴儿(IDM)。这是一种罕见的异常情况,其特征是大脑半球及额叶后部和顶叶区域其他脑结构的节段性分离失败,在“融合”区域前后的半球间裂正常。虽然与前脑无裂畸形(HPE)有明显重叠,但这种情况与HPE不同,MIF中的中线“融合”是完全但节段性的,而HPE谱系中所见的脑结构异常在从后向前的“融合”中严重程度呈平滑进展。然而,虽然MIF和HPE之间存在明显区别,但它们很可能源自相似的发病机制。因此,我们认为MIF是中线脑异常的HPE谱系的一种独特变体。鉴于已知IDM中HPE的发病率增加,MIF很可能是一种与母亲糖尿病相关的畸形。