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发热性惊厥相关变异。

Variants Associated with Febrile Seizures.

机构信息

Life Sciences Institute, University of Michigan, Ann Arbor, MI 48109, USA.

Department of Pediatrics, Seventh Medical Center of Chinese PLA General Hospital, Beijing 100010, China.

出版信息

Biomolecules. 2023 Feb 22;13(3):414. doi: 10.3390/biom13030414.

Abstract

Febrile seizures (FS) are the most common form of epilepsy in children between six months and five years of age. FS is a self-limited type of fever-related seizure. However, complicated prolonged FS can lead to complex partial epilepsy. We found that among the GABA receptor subunit () genes, most variants associated with FS are harbored in the γ2 subunit (). Here, we characterized the effects of eight variants in the GABA receptor γ2 subunit on receptor biogenesis and channel function. Two-thirds of the variants followed the expected autosomal dominant inheritance in FS and occurred as missense and nonsense variants. The remaining one-third appeared as de novo in the affected probands and occurred only as missense variants. The loss of GABA receptor function and dominant negative effect on GABA receptor biogenesis likely caused the FS phenotype. In general, variants in the result in a broad spectrum of phenotypic severity, ranging from asymptomatic, FS, genetic epilepsy with febrile seizures plus (GEFS+), and Dravet syndrome individuals. The data presented here support the link between FS, epilepsy, and variants, shedding light on the relationship between the variant topological occurrence and disease severity.

摘要

热性惊厥(FS)是 6 个月至 5 岁儿童中最常见的癫痫形式。FS 是一种自限性的发热相关惊厥。然而,复杂的长时间 FS 可导致复杂部分性癫痫。我们发现,在 GABA 受体亚基()基因中,与 FS 相关的大多数变体都位于 γ2 亚基()中。在这里,我们描述了 GABA 受体 γ2 亚基中 8 个变体对受体生物发生和通道功能的影响。FS 中,有三分之二的变体符合预期的常染色体显性遗传,表现为错义和无义变体。其余三分之一的变体在受影响的先证者中呈新生,仅表现为错义变体。GABA 受体功能的丧失和对 GABA 受体生物发生的显性负效应可能导致 FS 表型。一般来说, 中的变体导致表型严重程度的广泛范围,从无症状、FS、热性惊厥附加遗传(GEFS+)和 Dravet 综合征个体。这里呈现的数据支持 FS、癫痫和 变体之间的联系,阐明了变体拓扑发生与疾病严重程度之间的关系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88e9/10046037/1ef4d720256b/biomolecules-13-00414-g001.jpg

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