Guerrini R, Barkovich A J, Sztriha L, Dobyns W B
Division of Neurology, King's College, University of London, UK.
Neurology. 2000 Feb 22;54(4):909-13. doi: 10.1212/wnl.54.4.909.
Polymicrogyria is a brain malformation characterized by abnormal cortical lamination, excessive cortical folding, and fusion of the cortical molecular layer. Two distinct bilateral localized forms have been described: bilateral perisylvian polymicrogyria, which has proved to be genetically heterogeneous, and bilateral parasagittal parieto-occipital polymicrogyria, which has been described only in sporadic patients. We describe 13 patients with symmetric polymicrogyria of both frontal lobes back to the precentral sulcus: bilateral frontal polymicrogyria (BFP).
Review of clinical records, brain MRI, and EEG results of 13 patients; correlation with other regional polymicrogyrias.
The abnormal cortex extended from the frontal poles anteriorly to the precentral gyrus posteriorly and to the frontal operculum inferiorly and was relatively symmetric in all 13 patients. All patients presented with developmental delay and mild spastic quadriparesis, but variably impaired language development (12/13), mental retardation (11/13), and epilepsy (5/13) also occurred. BFP was sporadic in 13 of 13 patients, but 2 of 13 had consanguineous parents.
BFP extends the spectrum of the recognized bilateral symmetric regional polymicrogyria syndromes.
多小脑回是一种脑畸形,其特征为皮质分层异常、皮质过度折叠以及皮质分子层融合。已描述了两种不同的双侧局限性形式:双侧外侧裂周围多小脑回,已证实其具有遗传异质性;双侧矢状旁顶枕多小脑回,仅在散发病例中有描述。我们描述了13例额叶直至中央前沟均存在对称性多小脑回的患者:双侧额叶多小脑回(BFP)。
回顾13例患者的临床记录、脑部MRI和脑电图结果;与其他区域多小脑回进行相关性分析。
异常皮质从前额叶极向前延伸至中央前回,向后延伸至额下回,在所有13例患者中相对对称。所有患者均出现发育迟缓及轻度痉挛性四肢瘫,但语言发育受损情况各异(12/13),智力发育迟缓(11/13)以及癫痫(5/13)也有发生。13例患者中13例为散发病例,但13例中有2例父母为近亲结婚。
BFP扩展了已公认的双侧对称区域多小脑回综合征的范围。