Turner Samantha J, Morgan Angela T, Perez Eliane Roulet, Scheffer Ingrid E
Department of Paediatrics, The University of Melbourne, The Royal Children's Hospital, Parkville, Australia,
Curr Neurol Neurosci Rep. 2015 Jun;15(6):35. doi: 10.1007/s11910-015-0554-0.
The last 2 years have seen exciting advances in the genetics of Landau-Kleffner syndrome and related disorders, encompassed within the epilepsy-aphasia spectrum (EAS). The striking finding of mutations in the N-methyl-D-aspartate (NMDA) receptor subunit gene GRIN2A as the first monogenic cause in up to 20% of patients with EAS suggests that excitatory glutamate receptors play a key role in these disorders. Patients with GRIN2A mutations have a recognizable speech and language phenotype that may assist with diagnosis. Other molecules involved in RNA binding and cell adhesion have been implicated in EAS; copy number variations are also found. The emerging picture highlights the overlap between the genetic determinants of EAS with speech and language disorders, intellectual disability, autism spectrum disorders and more complex developmental phenotypes.
在过去两年中,兰道-克莱夫纳综合征及相关疾病的遗传学研究取得了令人振奋的进展,这些疾病都属于癫痫性失语谱系障碍(EAS)。在高达20%的EAS患者中,N-甲基-D-天冬氨酸(NMDA)受体亚基基因GRIN2A发生突变,这一惊人发现表明兴奋性谷氨酸受体在这些疾病中起关键作用。携带GRIN2A突变的患者具有可识别的言语和语言表型,这可能有助于诊断。其他参与RNA结合和细胞黏附的分子也与EAS有关;还发现了拷贝数变异。新出现的情况凸显了EAS的遗传决定因素与言语和语言障碍、智力残疾、自闭症谱系障碍以及更复杂的发育表型之间的重叠。