In vivo detection of pathologic α- synuclein and TDP-43 in the skin and olfactory mucosa of a patient with Parkinson’s disease-like phenotype carrying the p.Thr272Serfs*10 GRN mutation

IF 19.6 1区 医学 Q1 NEUROSCIENCES
Paola Caroppo,Vittoria Aprea,Cristina Villa,Ilaria Linda Dellarole,Aurora Romeo,Giacomina Rossi,Arianna Ciullini,Anna Burato,Sara Prioni,Marina Grisoli,Giuseppe Legname,Giulia Simmini,Alessia Luppino,Samanta Mazzetti,Fabio Moda,Grazia Devigili
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引用次数: 0

Abstract

Abstract We describe a patient carrying the GRN p.Thr272Serfs*10 mutation, who presented with parkinsonism at onset and later developed prodromal frontotemporal dementia, in whom seed amplification assay on olfactory mucosa and skin analyses suggest mixed TDP-43 and α-synuclein co-pathology, highlighting how combining these techniques could provide a comprehensive approach to investigate the underlying neuropathological process.
携带p.s thr272serfs *10 GRN突变的帕金森病样表型患者皮肤和嗅觉粘膜病理性α-突触核蛋白和TDP-43的体内检测
摘要我们描述了一名携带GRN p.s thr272serfs *10突变的患者,该患者发病时表现为帕金森病,后来发展为前驱额颞叶痴呆,其嗅觉粘膜和皮肤分析的种子扩增实验显示TDP-43和α-突触核蛋白混合病理,强调了如何将这些技术结合起来,可以提供一种全面的方法来研究潜在的神经病理过程。
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来源期刊
Molecular Neurodegeneration
Molecular Neurodegeneration 医学-神经科学
CiteScore
23.00
自引率
4.60%
发文量
78
审稿时长
6-12 weeks
期刊介绍: Molecular Neurodegeneration, an open-access, peer-reviewed journal, comprehensively covers neurodegeneration research at the molecular and cellular levels. Neurodegenerative diseases, such as Alzheimer's, Parkinson's, Huntington's, and prion diseases, fall under its purview. These disorders, often linked to advanced aging and characterized by varying degrees of dementia, pose a significant public health concern with the growing aging population. Recent strides in understanding the molecular and cellular mechanisms of these neurodegenerative disorders offer valuable insights into their pathogenesis.
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