Nissenkorn Andreea, Yosovich Keren, Leibovitz Zvi, Hartman Tamar Gur, Zelcer Itay, Hugirat Mohammad, Lev Dorit, Lerman-Sagie Tally, Blumkin Lubov
Metabolic Neurogenetic Service, 58883Wolfson Medical Center, Holon, Israel.
Pediatric Neurology Unit, 58883Wolfson Medical Center, Holon, Israel.
J Child Neurol. 2021 Jun;36(7):545-555. doi: 10.1177/0883073820984068. Epub 2021 Jan 8.
Congenital mirror movements are involuntary movements of a side of the body imitating intentional movements on the opposite side, appearing in early childhood and persisting beyond 7 years of age. Congenital mirror movements are usually idiopathic but have been reported in association with various brain malformations.
We describe clinical, genetic, and radiologic features in 9 individuals from 5 families manifesting congenital mirror movements.
The brain malformations associated with congenital mirror movements were: dysplastic corpus callosum in father and daughter with a heterozygous p.Met1* mutation in ; hypoplastic corpus callosum, dysgyria, and malformed vermis in a mother and son with a heterozygous p.Thr312Met mutation in ; dysplastic corpus callosum, dysgyria, abnormal vermis, and asymmetric ventricles in a father and 2 daughters with a heterozygous p.Arg121Trp mutation in hypoplastic corpus callosum, dysgyria, malformed basal ganglia and abnormal vermis in a patient with a heterozygous p.Glu155Asp mutation in ; hydrocephalus, hypoplastic corpus callosum, polymicrogyria, and cerebellar cysts in a patient with a homozygous p.Pro312Leu mutation in .
, cause abnormal axonal guidance via different mechanisms and result in congenital mirror movements associated with brain malformations.
先天性镜像运动是身体一侧的不自主运动,模仿另一侧的有意运动,出现在儿童早期,并持续到7岁以后。先天性镜像运动通常是特发性的,但也有与各种脑畸形相关的报道。
我们描述了来自5个家庭的9名表现出先天性镜像运动的个体的临床、遗传和放射学特征。
与先天性镜像运动相关的脑畸形有:父女患有发育异常的胼胝体,存在杂合子p.Met1*突变;母子患有胼胝体发育不全、脑回发育异常和小脑蚓部畸形,存在杂合子p.Thr312Met突变;父子及两个女儿患有发育异常的胼胝体、脑回发育异常、异常的小脑蚓部和不对称的脑室,存在杂合子p.Arg121Trp突变;一名患者患有胼胝体发育不全、脑回发育异常、基底神经节畸形和异常的小脑蚓部,存在杂合子p.Glu155Asp突变;一名患者患有脑积水、胼胝体发育不全、多小脑回畸形和小脑囊肿,存在纯合子p.Pro312Leu突变。
, 通过不同机制导致异常的轴突导向,从而导致与脑畸形相关的先天性镜像运动。