Clinical Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt.
Pediatric Department, Faculty of Medicine, Cairo University, Cairo, Egypt.
J Hum Genet. 2022 Nov;67(11):669-673. doi: 10.1038/s10038-022-01060-x. Epub 2022 Jul 27.
Developmental brain malformations are rare but are increasingly reported features of BICD2-related disorders. Here, we report a 2-year old boy with microcephaly, profound delay and partial seizures. His brain MRI showed lissencephaly, hypogenesis of corpus callosum, dysplastic hipocampus and cerebellar hypoplasia. Whole-exome sequencing identified a novel homozygous likely pathogenic variant in the BICD2 gene, c.229 C > T p.(Gln77Ter). This is the first report of lissencephaly and cerebellar hypoplasia seen in a patient with homozygous loss-of-function variant in BICD2 that recapitulated the animal model. Our report supports that BICD2 should be considered in the differential diagnosis for patients with lissencephaly and cerebellar hypoplasia Additional clinical features of BICD2 are likely to emerge with the identification of additional patients.
脑发育畸形较为罕见,但越来越多的研究表明 BICD2 相关疾病存在该特征。本研究报道了一例 2 岁男孩,表现为小头畸形、严重发育迟缓伴部分性癫痫发作。头颅 MRI 显示无脑回畸形、胼胝体发育不全、海马发育不良和小脑发育不良。全外显子组测序发现 BICD2 基因的一个新的纯合可能致病性变异 c.229 C > T p.(Gln77Ter)。这是首例报道 BICD2 纯合功能丧失变异导致的无脑回畸形和小脑发育不良患者,该患者的临床表现与动物模型相吻合。本研究提示,对于无脑回畸形和小脑发育不良患者,应考虑 BICD2 作为鉴别诊断。随着更多患者的发现,可能会出现 BICD2 的其他临床特征。