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本文引用的文献

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Gross Motor Function in Pediatric Onset -Related Leukodystrophy: GMFM-88 Performance and Validation of GMFC-MLD in .儿科起病相关性脑白质营养不良的粗大运动功能:GMFM-88 的表现及 GMFC-MLD 的验证。
J Child Neurol. 2023 Aug;38(8-9):498-504. doi: 10.1177/08830738231188159. Epub 2023 Jul 17.
2
Neurodegeneration with brain iron accumulation: a case series highlighting phenotypic and genotypic diversity in 20 Indian families.伴有脑铁蓄积的神经退行性变:20 个印度家系中表型和基因型多样性的病例系列。
Neurogenetics. 2023 Apr;24(2):113-127. doi: 10.1007/s10048-023-00712-0. Epub 2023 Feb 15.
3
Lifetime risk of autosomal recessive neurodegeneration with brain iron accumulation (NBIA) disorders calculated from genetic databases.从遗传数据库计算常染色体隐性遗传性伴脑铁沉积的神经退行性疾病(NBIA)的终生风险。
EBioMedicine. 2022 Mar;77:103869. doi: 10.1016/j.ebiom.2022.103869. Epub 2022 Feb 15.
4
Neurodegeneration with brain iron accumulation: Characterization of clinical, radiological, and genetic features of pediatric patients from Southern India.神经退行性脑铁蓄积症:来自印度南部的儿科患者的临床、影像学和遗传学特征的描述。
Brain Dev. 2021 Nov;43(10):1013-1022. doi: 10.1016/j.braindev.2021.06.010. Epub 2021 Jul 14.
5
Treat Iron-Related Childhood-Onset Neurodegeneration (TIRCON)-An International Network on Care and Research for Patients With Neurodegeneration With Brain Iron Accumulation (NBIA).治疗与铁相关的儿童期起病神经退行性变(TIRCON)——脑铁沉积神经退行性变(NBIA)患者护理与研究国际网络。
Front Neurol. 2021 Feb 22;12:642228. doi: 10.3389/fneur.2021.642228. eCollection 2021.
6
Is there heart disease in cases of neurodegeneration associated with mutations in C19orf12?与 C19orf12 突变相关的神经退行性变中是否存在心脏病?
Parkinsonism Relat Disord. 2020 Nov;80:15-18. doi: 10.1016/j.parkreldis.2020.09.014. Epub 2020 Sep 8.
7
Minimum Clinically Important Difference of Gross Motor Function and Gait Endurance in Children with Motor Impairment: A Comparison of Distribution-Based Approaches.运动障碍儿童粗大运动功能和步态耐力的最小临床重要差异:基于分布的方法比较。
Biomed Res Int. 2020 May 15;2020:2794036. doi: 10.1155/2020/2794036. eCollection 2020.
8
Palliative care in 9 children with neurodegeneration with brain iron accumulation.神经退行性脑铁蓄积症 9 例患儿的姑息治疗。
Neurol Sci. 2020 Mar;41(3):653-660. doi: 10.1007/s10072-019-04099-5. Epub 2019 Nov 22.
9
Botulinum Toxin-A Injection in the Treatment of Spasticity in a Infantile-Onset Neurodegeneration With Brain Iron Accumulation: A Case Report.A型肉毒毒素注射治疗婴儿期起病的脑铁沉积神经退行性疾病中的痉挛:一例报告
Ann Rehabil Med. 2018 Apr;42(2):363-367. doi: 10.5535/arm.2018.42.2.363. Epub 2018 Apr 30.
10
Classification and molecular pathogenesis of NBIA syndromes.NBIA 综合征的分类和分子发病机制。
Eur J Paediatr Neurol. 2018 Mar;22(2):272-284. doi: 10.1016/j.ejpn.2018.01.008. Epub 2018 Jan 17.

神经退行性脑铁沉积症患者的功能障碍:初步结果。

Functional impairments in NBIA patients: Preliminary results.

作者信息

Syczewska Małgorzata, Stęplowska Anna, Szczerbik Ewa, Kalinowska Małgorzata, Cwyl Maciej

机构信息

Department of Rehabilitation, The Children's Memorial Health Institute, Warszawa, Poland.

Olinek, Warszawa, Poland.

出版信息

Intractable Rare Dis Res. 2024 Aug 31;13(3):172-177. doi: 10.5582/irdr.2024.01019.

DOI:10.5582/irdr.2024.01019
PMID:39220277
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11350201/
Abstract

Neurodegeneration with brain iron accumulation (NBIA) is a heterogeneous group (genetically and phenotypically) of genetically determined disorders. Up to date there is no cure for this disease, so the applied treatments focus on symptoms control and palliative care. The main problems are delayed motor development, gait deterioration, postural instability, cognitive dysfunctions, abnormal muscle tone and many others. As gait and balance deficits are predominant features of NBIA patients this study aimed at the use of the objective, instrumented functional tests as well as functional assessment scales to assess their functional impairments. Twenty three NBIA patients recruited for the study underwent objective, instrumented gait analysis, balance assessment, pedobarography and functional evaluation with Gross Motor Function Measure (GMFM-88). The results showed high variability and heterogeneity of NBIA functional status (GMFM from 27.5 to 100.0), but also showed some differences in gait pattern between their types ( < 0.05 at the pelvis, hip and knee). We think that these results could help design objective assessment protocols in future clinical studies.

摘要

脑铁沉积神经退行性变(NBIA)是一组由基因决定的疾病(在遗传和表型上),具有异质性。到目前为止,这种疾病尚无治愈方法,因此应用的治疗方法主要集中在症状控制和姑息治疗上。主要问题包括运动发育迟缓、步态恶化、姿势不稳、认知功能障碍、肌张力异常等。由于步态和平衡缺陷是NBIA患者的主要特征,本研究旨在使用客观的、仪器化的功能测试以及功能评估量表来评估他们的功能障碍。招募的23名NBIA患者接受了客观的、仪器化的步态分析、平衡评估、足底压力测量以及使用粗大运动功能测量量表(GMFM - 88)进行功能评估。结果显示NBIA功能状态具有高度变异性和异质性(GMFM从27.5到100.0),但不同类型之间在步态模式上也存在一些差异(骨盆、髋部和膝部P<0.05)。我们认为这些结果有助于在未来的临床研究中设计客观的评估方案。