Chang B S, Apse K A, Caraballo R, Cross J H, Mclellan A, Jacobson R D, Valente K D, Barkovich A J, Walsh C A
Department of Neurology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.
Neurology. 2006 Jan 10;66(1):133-5. doi: 10.1212/01.wnl.0000191393.06679.e9.
A number of familial syndromes of bilateral polymicrogyria (PMG) have been described, but reported unilateral PMG cases have generally been sporadic. The authors identified four families in which unilateral right-sided PMG on MRI was present in more than one individual, with pathologic confirmation in one. Core clinical features included contralateral hemiparesis, developmental delay, and focal seizures. The authors' findings suggest that unilateral PMG exists in a familial syndrome of probable germline genetic origin.
已经描述了一些双侧多小脑回畸形(PMG)的家族性综合征,但报告的单侧PMG病例通常为散发性。作者发现了四个家族,其中不止一人在MRI上表现为右侧单侧PMG,其中一个家族有病理证实。核心临床特征包括对侧偏瘫、发育迟缓以及局灶性癫痫发作。作者的研究结果表明,单侧PMG存在于一种可能起源于种系基因的家族性综合征中。