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Neuropathology of sporadic Parkinson's disease: Evaluation and changes of concepts

โœ Scribed by Kurt A. Jellinger


Book ID
102945934
Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
725 KB
Volume
27
Category
Article
ISSN
0885-3185

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โœฆ Synopsis


Abstract

Parkinson's disease (PD), one of the most frequent neurodegenerative disorders, is no longer considered a complex motor disorder characterized by extrapyramidal symptoms, but a progressive multisystem orโ€”more correctlyโ€”multiorgan disease with variegated neurological and nonmotor deficiencies. It is morphologically featured not only by the degeneration of the dopaminergic nigrostriatal system, responsible for the core motor deficits, but by multifocal involvement of the central, peripheral and autonomic nervous system and other organs associated with widespread occurrence of Lewy bodies and dystrophic Lewy neurites. This results from deposition of abnormal ฮฑโ€synuclein (ฮฑSyn), the major protein marker of PD, and other synucleinopathies. Recent research has improved both the clinical and neuropathological diagnostic criteria of PD; it has further provided insights into the development and staging of ฮฑSyn and Lewy pathologies and has been useful in understanding the pathogenesis of PD. However, many challenges remain, for example, the role of Lewy bodies and the neurobiology of axons in the course of neurodegeneration, the relation between ฮฑSyn, Lewy pathology, and clinical deficits, as well as the interaction between ฮฑSyn and other pathologic proteins. Although genetic and experimental models have contributed to exploring the causes, pathomechanisms, and treatment options of PD, there is still a lack of an optimal animal model, and the etiology of this devastating disease is far from being elucidated. ยฉ 2011 Movement Disorder Society


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