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PURA-NDD 的神经肌肉和神经肌肉接头表现:已报道症状和潜在治疗选择的系统综述。

Neuromuscular and Neuromuscular Junction Manifestations of the PURA-NDD: A Systematic Review of the Reported Symptoms and Potential Treatment Options.

机构信息

Center for Cardiovascular Genetics & Gene Diagnostics, Foundation for People with Rare Diseases, 8952 Schlieren, Switzerland.

Division of Neurology, Johns Hopkins All Children's Hospital, 501 6th Ave S, St. Petersburg, FL 33701, USA.

出版信息

Int J Mol Sci. 2023 Jan 23;24(3):2260. doi: 10.3390/ijms24032260.

DOI:10.3390/ijms24032260
PMID:36768582
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9917016/
Abstract

PURA-related neurodevelopmental disorders (PURA-NDDs) are a rare genetic disease caused by pathogenic autosomal dominant variants in the PURA gene or a deletion encompassing the PURA gene. PURA-NDD is clinically characterized by neurodevelopmental delay, learning disability, neonatal hypotonia, feeding difficulties, abnormal movements, and epilepsy. It is generally considered to be central nervous system disorders, with generalized weakness, associated hypotonia, cognitive and development deficits in early development, and seizures in late stages. Although it is classified predominantly as a central nervous syndrome disorder, some phenotypic features, such as myopathic facies, respiratory insufficiency of muscle origin, and myopathic features on muscle biopsy and electrodiagnostic evaluation, point to a peripheral (neuromuscular) source of weakness. Patients with PURA-NDD have been increasingly identified in exome-sequenced cohorts of patients with neuromuscular- and congenital myasthenic syndrome-like phenotypes. Recently, fluctuating weakness noted in a PURA-NDD patient, accompanied by repetitive nerve stimulation abnormalities, suggested the disease to be a channelopathy and, more specifically, a neuromuscular junction disorder. Treatment with pyridostigmine or salbutamol led to clinical improvement of neuromuscular function in two reported cases. The goal of this systematic retrospective review is to highlight the motor symptoms of PURA-NDD, to further describe the neuromuscular phenotype, and to emphasize the role of potential treatment opportunities of the neuromuscular phenotype in the setting of the potential role of PURA protein in the neuromuscular junction and the muscles.

摘要

PURA 相关神经发育障碍(PURA-NDD)是一种罕见的遗传性疾病,由 PURA 基因的致病性常染色体显性变异或包含 PURA 基因的缺失引起。PURA-NDD 的临床特征为神经发育迟缓、学习障碍、新生儿低张力、喂养困难、运动异常和癫痫。它通常被认为是中枢神经系统疾病,具有全身无力、相关低张力、早期发育认知和发育缺陷以及后期癫痫发作的特点。尽管它主要被归类为中枢综合征障碍,但一些表型特征,如肌病面容、肌肉源性呼吸功能不全和肌肉活检和电诊断评估中的肌病特征,提示存在周围(神经肌肉)来源的无力。在神经肌肉和先天性肌无力综合征样表型的外显子组测序队列中,越来越多的患者被发现患有 PURA-NDD。最近,一名 PURA-NDD 患者出现波动性无力,并伴有重复神经刺激异常,提示该病为通道病,更具体地说,是神经肌肉接头疾病。在报告的两例病例中,使用吡啶斯的明或沙丁胺醇治疗导致神经肌肉功能的临床改善。本系统回顾性研究的目的是强调 PURA-NDD 的运动症状,进一步描述神经肌肉表型,并强调神经肌肉表型的潜在治疗机会在 PURA 蛋白在神经肌肉接头和肌肉中的潜在作用背景下的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50c3/9917016/8a976e8a6dcb/ijms-24-02260-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50c3/9917016/36c5c34101d6/ijms-24-02260-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50c3/9917016/8a976e8a6dcb/ijms-24-02260-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50c3/9917016/36c5c34101d6/ijms-24-02260-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50c3/9917016/8a976e8a6dcb/ijms-24-02260-g002.jpg

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引用本文的文献

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PURA syndrome-a genetic cause of a neurodevelopmental disorder-case report.普拉综合征——一种神经发育障碍的遗传病因——病例报告
Front Pediatr. 2025 Jul 10;13:1607213. doi: 10.3389/fped.2025.1607213. eCollection 2025.
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Congenital myasthenic syndromes: increasingly complex.先天性肌无力综合征:越来越复杂。

本文引用的文献

1
A 25 Mainland Chinese cohort of patients with PURA-related neurodevelopmental disorders: clinical delineation and genotype-phenotype correlations.一个涉及 25 名中国大陆 PURA 相关神经发育障碍患者的队列:临床特征及基因型-表型相关性。
Eur J Hum Genet. 2023 Jan;31(1):112-121. doi: 10.1038/s41431-022-01217-4. Epub 2022 Nov 14.
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PURA syndrome: neuromuscular junction manifestations with potential therapeutic implications.PURA 综合征:具有潜在治疗意义的神经肌肉接头表现。
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Heterozygous c.175C>T variant in gene causes severe developmental delay.基因中的杂合c.175C>T变异导致严重发育迟缓。
Clin Case Rep. 2023 Sep 7;11(9):e7779. doi: 10.1002/ccr3.7779. eCollection 2023 Sep.
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PURA syndrome in a child with severe developmental delay: a challenging diagnosis.儿童严重发育迟缓伴 PURA 综合征:一项具有挑战性的诊断。
Rev Neurol. 2022 Mar 1;74(5):170-173. doi: 10.33588/rn.7405.2021068.
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Hypotonic infant with PURA syndrome-related channelopathy successfully treated with pyridostigmine.患有与PURA综合征相关的通道病的低渗性婴儿用吡啶斯的明成功治疗。
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Related Developmental and Epileptic Encephalopathy: Phenotypic and Genotypic Spectrum.相关发育性和癫痫性脑病:表型和基因型谱
Neurol Genet. 2021 Nov 15;7(6):e613. doi: 10.1212/NXG.0000000000000613. eCollection 2021 Dec.
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Complex Movement Disorders in a Boy with PURA Syndrome.一名患有PURA综合征男孩的复杂运动障碍
Mov Disord Clin Pract. 2021 Jul 8;8(7):1137-1139. doi: 10.1002/mdc3.13272. eCollection 2021 Oct.
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Early-onset bradykinetic rigid syndrome and reflex seizures in a child with PURA syndrome.一名患有PURA综合征的儿童出现早发性运动迟缓僵硬综合征和反射性癫痫发作。
Epileptic Disord. 2021 Oct 1;23(5):745-748. doi: 10.1684/epd.2021.1328.
9
4-Aminopyridine is a promising treatment option for patients with gain-of-function -encephalopathy.4-氨基吡啶是治疗功能获得性脑病患者的一种有前途的治疗选择。
Sci Transl Med. 2021 Sep;13(609):eaaz4957. doi: 10.1126/scitranslmed.aaz4957. Epub 2021 Sep 1.
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The PRISMA 2020 statement: an updated guideline for reporting systematic reviews.《PRISMA 2020声明:系统评价报告的更新指南》
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