Literature DB >> 12518300

Limb-kinetic apraxia in corticobasal degeneration: clinical and kinematic features.

Ramón C Leiguarda1, Marcelo Merello, María Inés Nouzeilles, Jorge Balej, Alberto Rivero, Martín Nogués.   

Abstract

Current concepts regarding the organisation of the motor system indicate the existence of a frontoparietal circuit involved in prehension and manipulation, whose damage may result in a motor behavioural disorder strongly resembling the one originally described as limb-kinetic apraxia. To determine the specific clinical and kinematic features of this distinctive praxic disorder, 5 patients with corticobasal degeneration (apraxic group), 5 with Parkinson's disease (nonapraxic group), and 10 control subjects were studied by a comprehensive apraxic battery, three-dimensional motion analysis of manipulative movements and motor evoked potentials. A mathematical model [quality of movement coefficient (QMC)] was applied to quantify differential kinematic characteristics between elementary motor deficits and the praxic disorder. Transcranial magnetic stimulation was used to evaluate corticomotoneural projections and cortical inhibition. All five patients in the apraxic group exhibited a unilateral praxic deficit characterised by derangement of fractionated and segmental finger movements. QMC was significantly greater in apraxic than in nonapraxic patients (P < 0.02), revealing a chaotic movement with marked interfinger uncoordination. Conventional transcranial magnetic stimulation parameters were within normal limits in both groups of patients; however, the silent period was significantly shorter in the apraxic limb when compared with control subjects (P < 0.001). Limb-kinetic apraxia is a distinctive disorder affecting the performance of finger and hand postures and movements over and above a corticospinal or basal ganglion deficit. Disruption of the frontoparietal circuit devoted to grasping and manipulation, together with defective cortical inhibition, which would also interfere with the selection and control of hand muscle activity, are the most likely underlying physiopathological mechanisms of limb-kinetic apraxia in patients with corticobasal degeneration. Copyright 2002 Movement Disorder Society

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Year:  2003        PMID: 12518300     DOI: 10.1002/mds.10303

Source DB:  PubMed          Journal:  Mov Disord        ISSN: 0885-3185            Impact factor:   10.338


  12 in total

Review 1.  Extrapyramidal syndromes in frontotemporal degeneration.

Authors:  Andrew Kertesz; Paul McMonagle; Sarah Jesso
Journal:  J Mol Neurosci       Date:  2011-09-02       Impact factor: 3.444

Review 2.  Neurophysiology and neurochemistry of corticobasal syndrome.

Authors:  Aditya A Murgai; Mandar S Jog
Journal:  J Neurol       Date:  2018-01-06       Impact factor: 4.849

Review 3.  [Apraxia--neuroscience and clinical aspects. A literature synthesis].

Authors:  T Platz
Journal:  Nervenarzt       Date:  2005-10       Impact factor: 1.214

Review 4.  Transcranial Magnetic Stimulation for the Assessment of Neurodegenerative Disease.

Authors:  Steve Vucic; Matthew C Kiernan
Journal:  Neurotherapeutics       Date:  2017-01       Impact factor: 7.620

Review 5.  Update on apraxia.

Authors:  Rachel Goldmann Gross; Murray Grossman
Journal:  Curr Neurol Neurosci Rep       Date:  2008-11       Impact factor: 5.081

Review 6.  Safety of transcranial magnetic stimulation in Parkinson's disease: a review of the literature.

Authors:  Matthew Vonloh; Robert Chen; Benzi Kluger
Journal:  Parkinsonism Relat Disord       Date:  2013-03-07       Impact factor: 4.891

Review 7.  A model-based approach to understanding apraxia in Corticobasal Syndrome.

Authors:  Vessela Stamenova; Eric A Roy; Sandra E Black
Journal:  Neuropsychol Rev       Date:  2008-12-11       Impact factor: 7.444

8.  An unusual cause of dementia: essential diagnostic elements of corticobasal degeneration-a case report and review of the literature.

Authors:  F Mastrolilli; A Benvenga; L Di Biase; F Giambattistelli; L Trotta; G Salomone; L Quintiliani; D Landi; J M Melgari; F Vernieri
Journal:  Int J Alzheimers Dis       Date:  2011-07-12

9.  Progression of logopenic variant primary progressive aphasia to apraxia and semantic memory deficits.

Authors:  Michitaka Funayama; Yoshitaka Nakagawa; Yoko Yamaya; Fumihiro Yoshino; Masaru Mimura; Motoichiro Kato
Journal:  BMC Neurol       Date:  2013-11-01       Impact factor: 2.474

10.  The c.429_452 duplication of the ARX gene: a unique developmental-model of limb kinetic apraxia.

Authors:  Aurore Curie; Tatjana Nazir; Amandine Brun; Yves Paulignan; Anne Reboul; Karine Delange; Anne Cheylus; Sophie Bertrand; Fanny Rochefort; Gérald Bussy; Stéphanie Marignier; Didier Lacombe; Catherine Chiron; Mireille Cossée; Bruno Leheup; Christophe Philippe; Vincent Laugel; Anne De Saint Martin; Silvia Sacco; Karine Poirier; Thierry Bienvenu; Isabelle Souville; Brigitte Gilbert-Dussardier; Eric Bieth; Didier Kauffmann; Philippe Briot; Bénédicte de Fréminville; Fabienne Prieur; Michel Till; Caroline Rooryck-Thambo; Isabelle Mortemousque; Isabelle Bobillier-Chaumont; Annick Toutain; Renaud Touraine; Damien Sanlaville; Jamel Chelly; Sonya Freeman; Jian Kong; Nouchine Hadjikhani; Randy L Gollub; Alice Roy; Vincent des Portes
Journal:  Orphanet J Rare Dis       Date:  2014-02-14       Impact factor: 4.123

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