Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, 77030.
Department of Pediatrics, Faculty of Medicine, Kuwait University, P.O. Box 24923, 13110, Safat, Kuwait.
Ann Clin Transl Neurol. 2020 May;7(5):610-627. doi: 10.1002/acn3.51003. Epub 2020 Apr 14.
Defects in ion channels and neurotransmitter receptors are implicated in developmental and epileptic encephalopathy (DEE). Metabotropic glutamate receptor 7 (mGluR7), encoded by GRM7, is a presynaptic G-protein-coupled glutamate receptor critical for synaptic transmission. We previously proposed GRM7 as a candidate disease gene in two families with neurodevelopmental disorders (NDDs). One additional family has been published since. Here, we describe three additional families with GRM7 biallelic variants and deeply characterize the associated clinical neurological and electrophysiological phenotype and molecular data in 11 affected individuals from six unrelated families.
Exome sequencing and family-based rare variant analyses on a cohort of 220 consanguineous families with NDDs revealed three families with GRM7 biallelic variants; three additional families were identified through literature search and collaboration with a clinical molecular laboratory.
We compared the observed clinical features and variants of 11 affected individuals from the six unrelated families. Identified novel deleterious variants included two homozygous missense variants (c.2671G>A:p.Glu891Lys and c.1973G>A:p.Arg685Gln) and one homozygous stop-gain variant (c.1975C>T:p.Arg659Ter). Developmental delay, neonatal- or infantile-onset epilepsy, and microcephaly were universal. Three individuals had hypothalamic-pituitary-axis dysfunction without pituitary structural abnormality. Neuroimaging showed cerebral atrophy and hypomyelination in a majority of cases. Two siblings demonstrated progressive loss of myelination by 2 years in both and an acquired microcephaly pattern in one. Five individuals died in early or late childhood.
Detailed clinical characterization of 11 individuals from six unrelated families demonstrates that rare biallelic GRM7 pathogenic variants can cause DEEs, microcephaly, hypomyelination, and cerebral atrophy.
离子通道和神经递质受体的缺陷与发育性和癫痫性脑病(DEE)有关。代谢型谷氨酸受体 7(mGluR7)由 GRM7 编码,是一种关键的突触前 G 蛋白偶联谷氨酸受体,对突触传递至关重要。我们之前曾提出 GRM7 是两个神经发育障碍(NDD)家族的候选疾病基因。此后又发表了一个额外的家族。在这里,我们描述了另外三个具有 GRM7 双等位基因变异的家族,并对来自六个无关家族的 11 名受影响个体的相关临床神经和电生理表型以及分子数据进行了深入分析。
对 220 个具有 NDD 的近亲家庭的外显子组测序和基于家族的罕见变异分析显示,有三个家族存在 GRM7 双等位基因变异;通过文献检索和与临床分子实验室的合作,又确定了另外三个家族。
我们比较了六个无关家族的 11 名受影响个体的观察到的临床特征和变异。鉴定出的新的有害变异包括两个纯合错义变异(c.2671G>A:p.Glu891Lys 和 c.1973G>A:p.Arg685Gln)和一个纯合终止变异(c.1975C>T:p.Arg659Ter)。发育迟缓、新生儿或婴儿期起病的癫痫发作和小头畸形是普遍存在的。三个人存在下丘脑-垂体轴功能障碍,而没有垂体结构异常。神经影像学显示大多数病例存在脑萎缩和少突胶质细胞发育不良。两名兄弟姐妹在 2 岁时均出现髓鞘化进行性丢失,其中一名出现获得性小头畸形。五人在儿童早期或晚期死亡。
对六个无关家族的 11 名个体进行详细的临床特征分析表明,罕见的双等位基因 GRM7 致病性变异可导致 DEE、小头畸形、少突胶质细胞发育不良和脑萎缩。