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PACS 基因家族相关神经疾病:有限的基因型与多样的表型。

PACS gene family-related neurological diseases: limited genotypes and diverse phenotypes.

机构信息

Department of Pediatrics, Peking University First Hospital, No. 1 Xi'an Men Street, West District, Beijing, 100034, China.

Beijing Key Laboratory of Molecular Diagnosis and Study on Pediatric Genetic Diseases, Beijing, China.

出版信息

World J Pediatr. 2024 Jan;20(1):82-91. doi: 10.1007/s12519-022-00652-z. Epub 2023 Jan 16.

Abstract

BACKGROUND

The PACS gene family has been demonstrated to be related to intracellular vesicular trafficking. The phenotypic manifestations caused by the pathogenic variants of PACS include epilepsy, intellectual disability/developmental delay, and malformations, such as facial abnormalities.

METHODS

We identified seven new cases with pathogenic or likely pathogenic PACS variants using next-generation sequencing. Detailed information obtained from these patients was analyzed along with that obtained from previously reported patients.

RESULTS

With the inclusion of the newly diagnosed cases in this study, 103 cases with PACS gene family-related neurological diseases were reported, of which 43 were PACS2-related cases and the remaining were PACS1-related cases. Most patients had seizures, which have been reported to be effectively controlled by several types of anti-seizure medications (ASMs). The most efficacious and frequently prescribed ASMs included sodium valproate (43.3%, 13/30), oxcarbazepine/carbamazepine (26.7%, 8/30), and levetiracetam (20%, 6/30). Almost all patients had intellectual disability/developmental delay. The most common pathogenic missense variants were PACS1 p. Arg203Trp and PACS2 p.Glu209Lys. In addition, we report a patient carrying a likely pathogenic copy number variation (CNV) (de novo heterozygous deletion of chr14:105821380-106107443, 286 kilobase, destroyed part of the furin-binding region domain and the protein structure after it) with more severe and refractory late-onset epilepsy.

CONCLUSIONS

The clinical phenotypes of the different PACS heterozygous missense variants were similar. The pathogenic variant sites of PACS1 and PACS2 were quite limited but located in different regions. A CNV destroying part of the PACS2 gene might also be pathogenic. These findings may provide an important clue for further functional studies on the pathogenic mechanism of neurological disorders related to the PACS gene family. Video Abstract (MP4 65767 kb).

摘要

背景

PACS 基因家族与细胞内囊泡运输有关。PACS 致病性变异引起的表型表现包括癫痫、智力残疾/发育迟缓以及面部异常等畸形。

方法

我们使用下一代测序技术鉴定了 7 例具有致病性或可能致病性 PACS 变异的新病例。对这些患者的详细信息进行了分析,并与以前报道的患者的信息进行了比较。

结果

纳入本研究新诊断病例后,共报告了 103 例 PACS 基因家族相关神经疾病病例,其中 43 例为 PACS2 相关病例,其余为 PACS1 相关病例。大多数患者有癫痫发作,几种抗癫痫药物(ASMs)被报道能有效控制癫痫发作。最有效和经常开的 ASMs 包括丙戊酸钠(43.3%,13/30)、奥卡西平/卡马西平(26.7%,8/30)和左乙拉西坦(20%,6/30)。几乎所有患者都有智力残疾/发育迟缓。最常见的致病性错义变异为 PACS1 p.Arg203Trp 和 PACS2 p.Glu209Lys。此外,我们报告了一例携带可能致病性拷贝数变异(CNV)(chr14:105821380-106107443,286 千碱基,缺失 furin 结合区结构域和蛋白结构的新生杂合缺失)的患者,该患者癫痫发作更严重且更难治疗,发病较晚。

结论

不同 PACS 杂合错义变异的临床表型相似。PACS1 和 PACS2 的致病性变异位点非常有限,但位于不同区域。破坏 PACS2 基因部分的 CNV 也可能具有致病性。这些发现可能为进一步研究与 PACS 基因家族相关的神经发育障碍的致病机制提供重要线索。

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