Syntelencephaly in an infant of a diabetic mother

被引:0
|
作者
Robin, NH
Ko, LM
Heeger, S
Muise, KL
Judge, N
Bangert, BA
机构
[1] CASE WESTERN RESERVE UNIV, SCH MED, DEPT PEDIAT, CLEVELAND, OH 44106 USA
[2] CASE WESTERN RESERVE UNIV, SCH MED, DEPT OBSTET GYNECOL, CLEVELAND, OH 44106 USA
[3] CASE WESTERN RESERVE UNIV, SCH MED, DEPT RADIOL, CLEVELAND, OH 44106 USA
[4] UNIV HOSP CLEVELAND, CLEVELAND, OH USA
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1996年 / 66卷 / 04期
关键词
middle interhemispheric fusion; syntelencephaly; holoprosencephaly; midline brain malformation; infant of a diabetic mother;
D O I
10.1002/(SICI)1096-8628(19961230)66:4<433::AID-AJMG9>3.3.CO;2-0
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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 mechanism. 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. (C) 1996 Wiley-Liss, Inc.
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页码:433 / 437
页数:5
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