Lissencephaly with extreme cerebral and cerebellar hypoplasia. A magnetic resonance imaging study

被引：21

作者：

Kroon, AA

Smit, BJ

Barth, PG

Hennekam, RCM

机构：

[1] UNIV AMSTERDAM,ACAD MED CTR,DEPT PEDIAT,NL-1105 AZ AMSTERDAM,NETHERLANDS

[2] UNIV AMSTERDAM,ACAD MED CTR,DEPT NEUROL,NL-1105 AZ AMSTERDAM,NETHERLANDS

[3] UNIV AMSTERDAM,ACAD MED CTR,INST HUMAN GENET,NL-1105 AZ AMSTERDAM,NETHERLANDS

来源：

NEUROPEDIATRICS | 1996年 / 27卷 / 05期

关键词：

cerebellar hypoplasia; lissencephaly; microcephaly; microlissencephaly;

D O I：

10.1055/s-2007-973778

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

A newborn with a rare type of lissencephaly is reported, characterized by extreme cerebral and cerebellar hypoplasia. The diagnosis was made by postmortem mag magnetic resonance imaging, indicating the value of such studies to evaluate neuronal migration disorders in patients in whom autopsy cannot be performed. Two earlier described microlissencephaly syndromes, the ''Barth'' and ''McComb'' type, are reviewed.

引用

页码：273 / 276

页数：4