Parisi Pasquale, Miano Silvia, Mei Davide, Paolino Maria Chiara, Castaldo Rosa, Villa Maria Pia
Child Neurology, Paediatric Department, I Faculty of Medicine, La Sapienza University, Rome, Italy.
Brain Dev. 2010 Jun;32(6):511-5. doi: 10.1016/j.braindev.2009.06.007. Epub 2009 Jul 19.
Mutations of the DCX gene (Xp22.3) cause X-linked lissencephaly in males and double cortex syndrome (DCS) or subcortical band heterotopia (SBH) in females. SBH is characterized by bilateral bands of grey matter interposed in the white matter between the cortex and the lateral ventricles. The main clinical manifestation in patients with SBH is epilepsy, which may be partial or generalized and is intractable in approximately 65% of the patients. An association of periodic limb movements (PLMs) and SBH has not been documented previously. We describe a 2-year-old girl affected by SBH with epilepsy and periodic limb movements (PLMs), in whom a novel "de novo" missense substitution, Met1Val (M1V), was identified in the DCX gene. Physiopathological links between PLMs and SBH are discussed.
DCX基因(Xp22.3)突变在男性中会导致X连锁无脑回畸形,在女性中会导致双皮质综合征(DCS)或皮质下带异位(SBH)。SBH的特征是双侧灰质带夹在皮质与侧脑室之间的白质中。SBH患者的主要临床表现是癫痫,可为部分性或全身性,约65%的患者癫痫难以治疗。此前尚未有周期性肢体运动(PLM)与SBH相关联的记录。我们描述了一名2岁患有SBH且伴有癫痫和周期性肢体运动(PLM)的女孩,在其DCX基因中发现了一种新的“新生”错义替换,即Met1Val(M1V)。文中讨论了PLM与SBH之间的生理病理联系。