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表现为先天性偏瘫的先天性双侧外侧裂周围多小脑回畸形。

Congenital bilateral perisylvian polymicrogyria presenting as congenital hemiplegia.

作者信息

Miller S P, Shevell M, Rosenblatt B, Silver K, O'Gorman A, Andermann F

机构信息

Department of Neurology/Neurosurgery, McGill University, Montreal, Quebec, Canada.

出版信息

Neurology. 1998 Jun;50(6):1866-9. doi: 10.1212/wnl.50.6.1866.

DOI:10.1212/wnl.50.6.1866
PMID:9633745
Abstract

We report three children with pure congenital hemiplegia found to have congenital bilateral perisylvian polymicrogyria (CBPP). None of our patients had the seizures, oromotor dysfunction, or cognitive impairment usually associated with CBPP. CBPP may be more common and heterogeneous than previously thought, is easily recognized by MRI, and should be included in the differential diagnosis of the young child presenting with congenital hemiplegia.

摘要

我们报告了三名患有单纯先天性偏瘫的儿童,发现他们患有先天性双侧外侧裂周围多小脑回(CBPP)。我们的患者均没有通常与CBPP相关的癫痫发作、口运动功能障碍或认知障碍。CBPP可能比之前认为的更常见且具有异质性,通过磁共振成像(MRI)很容易识别,并且在患有先天性偏瘫的幼儿鉴别诊断中应予以考虑。

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Genetics of the polymicrogyria syndromes.多小脑回综合征的遗传学
J Med Genet. 2005 May;42(5):369-78. doi: 10.1136/jmg.2004.023952.
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