4.5 Article

Diagnosis across a cohort of atypical atypical and complex parkinsonism

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PARKINSONISM & RELATED DISORDERS
卷 111, 期 -, 页码 -

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ELSEVIER SCI LTD
DOI: 10.1016/j.parkreldis.2023.105408

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Atypical atypical parkinsonian syndromes; Complex parkinsonism; DCTN1; DiGeorge syndrome; L-2-hidroxiglutaric aciduria; Magnetic resonance parkinsonism index; MTP-AT6; Postencephalitic progressive supranuclear; palsy; Vascular progressive supranuclear palsy

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The diagnostic approach for adulthood parkinsonism is challenging when atypical features make it difficult to classify into Parkinson's disease or atypical parkinsonian syndromes (APS). This study retrospectively analyzed patients with a diagnosis of atypical APS and complex parkinsonism, and found distinctive non-neurodegenerative etiologies causing atypical and complex parkinsonism. Accurate clinical identification and distinction between neurodegenerative and non-neurodegenerative parkinsonism etiologies will allow for refining clinical trials. Rating: 8/10.
Introduction: The diagnostic approach for adulthood parkinsonism can be challenging when atypical features hamper its classification in one of the two main parkinsonian groups: Parkinson's disease or atypical parkin-sonian syndromes (APS). Atypical features are usually associated with non-sporadic neurodegenerative causes.Methods: Retrospective analysis of patients with a working clinical diagnosis of atypical APS and complex parkinsonism. Atypical APS were classified according to the diagnostic research criteria and the 4-step diagnostic approach (Stamelou et al. 2013). When not indicated, the final aetiological diagnosis was prospec-tively assessed. Brain MRI of progressive supranuclear palsy (PSP) look-alikes was reviewed by a neuroradiologist.Results: Among 18 patients enrolled, ten were assigned to the atypical APS and eight to the complex parkin-sonism group. In the atypical APS group, nine patients had PSP and one had corticobasal degeneration. In the PSP group the median magnetic resonance parkinsonism index was 17.1. A final aetiological diagnosis was established for 11 patients, four from the complex parkinsonism (L-2-hidroxiglutaric aciduria and DiGeorge syndrome) and seven from the atypical APS (Perry syndrome, postencephalitic PSP, vascular PSP, and MTP-AT6 mitochondrial disease) group.Conclusions: In this study, the identification of atypical APS features, as proposed in the 4-step diagnostic approach, successfully guided the investigation of alternative diagnoses. Distinctive non-neurodegenerative etiologies causing atypical atypical and complex parkinsonism were uncovered, including acquired (post -en-cephalitis and vascular) and genetic (MTP-AT6 mitochondrial disease mimicking PSP, described for the first time) ones. In the future, accurate clinical identification and distinction between neurodegenerative and non-neurodegenerative parkinsonism etiologies will allow for refining clinical trials.

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