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[皮质下板层异位症和无脑回畸形:X连锁遗传的脑畸形]

[Subcortical laminal heterotopia and lissencephaly: cerebral malformations of X-linked inheritance].

作者信息

Pinard J M, Desguerre I, Motte J, Dulac O, Ponsot G

机构信息

Service de Neuropédiatrie, Hôpital Saint Vincent-de-Paul, Paris, France.

出版信息

Rev Neurol (Paris). 1995 Mar;151(3):171-6.

PMID:7676153
Abstract

Subcortical laminar heterotopia (band heterotopia) is a brain malformation now recognized by MRI. We report 3 families (2 previously described) in which several members had subcortical laminar heterotopia or a more severe malformation (agyria/pachygyria). In these families, subcortical laminar heterotopia were observed in women and were associated with epilepsy or slight mental retardation depending on the extend of heterotopia. Males had lissencephaly with refractory epilepsy and severe mental retardation. The pedigrees of these families demonstrate that these 2 malformations originate from a single genetic origin. A single X-linked dominant gene is postulated. Diagnosis of subcortical laminar heterotopia in a female or lissencephaly in a male (except in the case of Miller-Dieker syndrome) requires appropriate genetic counselling in the family: brain imaging should be performed in relatives.

摘要

皮质下带状异位(又称带型异位)是一种目前可通过磁共振成像(MRI)识别的脑畸形。我们报告了3个家系(其中2个家系此前已有描述),这些家系中的几名成员患有皮质下带状异位或更严重的畸形(无脑回/巨脑回)。在这些家系中,皮质下带状异位见于女性,根据异位范围,与癫痫或轻度智力发育迟缓相关。男性则患有平滑脑并伴有难治性癫痫和严重智力发育迟缓。这些家系的谱系表明,这两种畸形起源于单一的遗传因素。推测存在一个X连锁显性基因。对于女性诊断为皮质下带状异位或男性诊断为平滑脑(米勒 - 迪克尔综合征情况除外),需要在家族中进行适当的遗传咨询:应对亲属进行脑成像检查。

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