Corticobasal syndrome: neuroimaging and neurophysiological advances.

atypical parkinsonism corticobasal degeneration corticobasal syndrome neuroimaging neurophysiology theta burst stimulation

Journal

European journal of neurology
ISSN: 1468-1331
Titre abrégé: Eur J Neurol
Pays: England
ID NLM: 9506311

Informations de publication

Date de publication:
May 2019
Historique:
received: 10 01 2019
accepted: 30 01 2019
pubmed: 6 2 2019
medline: 29 7 2020
entrez: 6 2 2019
Statut: ppublish

Résumé

Corticobasal degeneration (CBD) is a neurodegenerative condition characterized by 4R tau protein deposition in several brain regions that clinically manifests itself as a heterogeneous atypical parkinsonism typically expressed in adulthood. The prototypical clinical phenotype of CBD is corticobasal syndrome (CBS). Important insights into the pathophysiological mechanisms underlying motor and higher cortical symptoms in CBS have been gained by using advanced neuroimaging and neurophysiological techniques. Structural and functional neuroimaging studies often show asymmetric cortical and subcortical abnormalities, mainly involving perirolandic and parietal regions and basal ganglia structures. Neurophysiological investigations including electroencephalography and somatosensory evoked potentials provide useful information on the origin of myoclonus and on cortical sensory loss. Transcranial magnetic stimulation demonstrates heterogeneous and asymmetric changes in the excitability and plasticity of primary motor cortex and abnormal hemispheric connectivity. Neuroimaging and neurophysiological abnormalities in multiple brain areas reflect asymmetric neurodegeneration, leading to asymmetric motor and higher cortical symptoms in CBS.

Identifiants

pubmed: 30720235
doi: 10.1111/ene.13928
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

701-e52

Informations de copyright

© 2019 EAN.

Auteurs

F Di Stasio (F)

IRCCS Neuromed Institute, 'Sapienza' University of Rome, Pozzilli (Isernia), Italy.

A Suppa (A)

IRCCS Neuromed Institute, 'Sapienza' University of Rome, Pozzilli (Isernia), Italy.
Department of Human Neuroscience, 'Sapienza' University of Rome, Rome, Italy.

L Marsili (L)

Department of Human Neuroscience, 'Sapienza' University of Rome, Rome, Italy.

N Upadhyay (N)

Department of Human Neuroscience, 'Sapienza' University of Rome, Rome, Italy.

F Asci (F)

Department of Human Neuroscience, 'Sapienza' University of Rome, Rome, Italy.

M Bologna (M)

IRCCS Neuromed Institute, 'Sapienza' University of Rome, Pozzilli (Isernia), Italy.
Department of Human Neuroscience, 'Sapienza' University of Rome, Rome, Italy.

C Colosimo (C)

Department of Neurology, Santa Maria University Hospital, Terni, Italy.

G Fabbrini (G)

IRCCS Neuromed Institute, 'Sapienza' University of Rome, Pozzilli (Isernia), Italy.
Department of Human Neuroscience, 'Sapienza' University of Rome, Rome, Italy.

P Pantano (P)

IRCCS Neuromed Institute, 'Sapienza' University of Rome, Pozzilli (Isernia), Italy.
Department of Human Neuroscience, 'Sapienza' University of Rome, Rome, Italy.

A Berardelli (A)

IRCCS Neuromed Institute, 'Sapienza' University of Rome, Pozzilli (Isernia), Italy.
Department of Human Neuroscience, 'Sapienza' University of Rome, Rome, Italy.

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Classifications MeSH