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胎儿酒精综合征中的多小脑回畸形

Polymicrogyria in fetal alcohol syndrome.

作者信息

Reinhardt Konstanze, Mohr Alexander, Gärtner Jutta, Spohr Hans-Ludwig, Brockmann Knut

机构信息

Department of Pediatrics and Pediatric Neurology, University of Göttingen, Göttingen, Germany.

出版信息

Birth Defects Res A Clin Mol Teratol. 2010 Feb;88(2):128-31. doi: 10.1002/bdra.20629.

DOI:10.1002/bdra.20629
PMID:19764076
Abstract

BACKGROUND

Intrauterine exposure to alcohol may result in a distinct pattern of craniofacial abnormalities and central nervous system dysfunction, designated fetal alcohol syndrome (FAS). The spectrum of malformations of the brain associated with maternal alcohol abuse during pregnancy is much broader than the relatively uniform clinical phenotype of FAS. Among these malformations the most striking abnormalities involve the impairment of neuronal cell migration. However, polymicrogyria (PMG) has so far been reported only once in a human autopsy study of a child with FAS.

CASE

A 16-year-old girl with confirmed maternal alcohol consumption during pregnancy and full phenotype of FAS presented after two generalized epileptic seizures for neurologic assessment. Cranial magnetic resonance imaging revealed bilateral PMG in the superior frontal gyrus with asymmetric distribution. History, clinical features, and genetic investigations provided no evidence for any of the known genetic or acquired causes of PMG. Therefore, we propose that prenatal alcohol exposure is the cause of PMG in this patient rather than a mere coincidence.

CONCLUSION

Our observation represents only the second patient of PMG in FAS and confirms the phenotypic variability of cerebral malformations associated with maternal alcohol abuse during pregnancy. In patients with clinical features of FAS and neurologic deficits or seizures neuroimaging is recommended. Furthermore, FAS should be considered as a differential diagnosis for PMG.

摘要

背景

子宫内酒精暴露可能导致一种独特的颅面异常和中枢神经系统功能障碍模式,即胎儿酒精综合征(FAS)。孕期母亲酗酒相关的脑畸形谱比相对统一的FAS临床表型要广泛得多。在这些畸形中,最显著的异常涉及神经元细胞迁移受损。然而,到目前为止,在一项对患有FAS的儿童进行的人体尸检研究中仅报道过一次多小脑回(PMG)。

病例

一名16岁女孩,孕期母亲有饮酒史且具有典型的FAS表型,在两次全身性癫痫发作后前来进行神经学评估。头颅磁共振成像显示双侧额上回存在不对称分布的PMG。病史、临床特征及基因检测均未发现任何已知的导致PMG的遗传或后天性病因。因此,我们认为产前酒精暴露是该患者PMG的病因,而非单纯巧合。

结论

我们的观察结果表明这是FAS中第二例PMG患者,并证实了孕期母亲酗酒相关脑畸形的表型变异性。对于具有FAS临床特征及神经功能缺损或癫痫发作的患者,建议进行神经影像学检查。此外,FAS应被视为PMG的鉴别诊断之一。

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