Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
Division of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, WA, USA.
Mol Genet Genomic Med. 2021 Jan;9(1):e1542. doi: 10.1002/mgg3.1542. Epub 2020 Dec 22.
CTNNB1 (MIM 116806) encodes beta-catenin, an adherens junction protein that supports the integrity between layers of epithelial tissue and mediates intercellular signaling. Recently, various heterozygous germline variants in CTNNB1 have been associated with human disease, including neurodevelopmental disorder with spastic diplegia and visual defects (MIM 615075) as well as isolated familial exudative vitreoretinopathy without developmental delays or other organ system involvement (MIM 617572). From over 40 previously reported patients with CTNNB1-related neurodevelopmental disorder, many have had ocular anomalies including strabismus, hyperopia, and astigmatism. More recently, multiple reports indicate that these abnormalities are associated with the presence of vitreoretinopathy.
We gathered a cohort of three patients with CTNNB1-related neurodevelopmental disorder, recruited from both our own clinic and referred from outside providers. We then searched for a clinical database comprised of over 12,000 exome sequencing studies to identify and recruit four additional patients.
Here, we report seven new cases of CTNNB1-related neurodevelopmental disorder, all harboring de novo variants, six of which were previously unreported. All patients but one presented with a spectrum of ocular abnormalities and one patient, who was found to carry a missense variant in CTNNB1, had notable vitreoretinopathy.
Our findings suggest ophthalmologic screening should be performed in all patients with CTNNB1 variants.
CTNNB1(MIM 116806)编码β-连环蛋白,一种黏着连接蛋白,支持上皮组织层之间的完整性,并介导细胞间信号转导。最近,CTNNB1 中的各种杂合种系变异与人类疾病相关,包括伴有痉挛性双瘫和视觉缺陷的神经发育障碍(MIM 615075)以及不伴有发育迟缓或其他器官系统受累的孤立性家族性渗出性玻璃体视网膜病变(MIM 617572)。在超过 40 名先前报道的 CTNNB1 相关神经发育障碍患者中,许多患者有眼部异常,包括斜视、远视和散光。最近,多项报道表明这些异常与玻璃体视网膜病变的存在有关。
我们收集了一组 3 名 CTNNB1 相关神经发育障碍患者,这些患者来自我们自己的诊所和外部医疗机构。然后,我们搜索了一个由超过 12000 个外显子组测序研究组成的临床数据库,以识别和招募另外 4 名患者。
在这里,我们报告了 7 例新的 CTNNB1 相关神经发育障碍病例,所有病例均携带新生变异,其中 6 例为先前未报道的变异。除 1 例患者外,所有患者均表现出一系列眼部异常,而 1 例携带 CTNNB1 错义变异的患者则表现出明显的玻璃体视网膜病变。
我们的发现表明,应在所有携带 CTNNB1 变异的患者中进行眼科筛查。