The phenomenon of disproportionate antecollis in Parkinson's disease and multiple system atrophy
Identifieur interne : 002B31 ( Main/Exploration ); précédent : 002B30; suivant : 002B32The phenomenon of disproportionate antecollis in Parkinson's disease and multiple system atrophy
Auteurs : Bart P. C. Van De Warrenburg [Royaume-Uni, Pays-Bas] ; Carla Cordivari [Royaume-Uni] ; Aisling M. Ryan [Royaume-Uni] ; Rahul Phadke [Royaume-Uni] ; Janice L. Holton [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni] ; Mike G. Hanna [Royaume-Uni] ; Niall P. Quinn [Royaume-Uni]Source :
- Movement Disorders [ 0885-3185 ] ; 2007-12-15.
Descripteurs français
- Pascal (Inist)
English descriptors
- KwdEn :
- Aged, Antiparkinson Agents (therapeutic use), Botulinum Toxins, Type A (therapeutic use), Electromyography, Electrophysiology, Female, Fibrosis (pathology), Head, Humans, Levodopa (therapeutic use), Male, Middle Aged, Movement (physiology), Multiple System Atrophy (drug therapy), Multiple System Atrophy (pathology), Multiple System Atrophy (physiopathology), Multiple system atrophy, Muscle, Skeletal (pathology), Muscle, Skeletal (physiopathology), Myopathy, Neck, Nervous system diseases, Neuromuscular Agents (therapeutic use), Parkinson Disease (drug therapy), Parkinson Disease (pathology), Parkinson Disease (physiopathology), Parkinson disease, Parkinson's disease, antecollis, dropped head, multiple system atrophy, myopathy.
- MESH :
- chemical , therapeutic use : Antiparkinson Agents, Botulinum Toxins, Type A, Levodopa, Neuromuscular Agents.
- drug therapy : Multiple System Atrophy, Parkinson Disease.
- pathology : Fibrosis, Multiple System Atrophy, Muscle, Skeletal, Parkinson Disease.
- physiology : Movement.
- physiopathology : Multiple System Atrophy, Muscle, Skeletal, Parkinson Disease.
- Aged, Electromyography, Electrophysiology, Female, Head, Humans, Male, Middle Aged, Neck.
Abstract
We sought to explore the phenomenon of disproportionate antecollis in multiple system atrophy (MSA) and Parkinson's disease (PD). The etiology is much debated and the main issue is whether it represents a primary myopathy or is secondary to the underlying motor disorder. The clinical, electrophysiological, and biopsy data of MSA or PD patients with antecollis were reviewed. We reviewed 16 patients (7 MSA and 9 PD) who developed antecollis during the course of their disease. The interval between onset of motor symptoms and of antecollis was shorter in the MSA group (4.6 ± 1.7 years vs. 10.5 ± 7.0 years). In 6 patients, the antecollis developed subacutely, and in 2 the abnormal neck flexion was initially an off‐period phenomenon. Two additional patients also showed some dopa‐responsiveness. Clinically, the antecollis was characterized by a forward flexion and anterior shift of the neck, with prominent cervical paraspinal and levator scapulae muscles, usually without weakness of residual neck extension. Electromyography of cervical paraspinal muscles showed mixed myopathic, normal, and neurogenic units, without early recruitment. Cervical paraspinal muscle biopsy in 2 patients disclosed fibrosis and nonspecific myopathic changes. We suggest that, in the context of MSA or PD, the initiating event in antecollis could be a disproportionately increased tone in anterior neck muscles that leads to secondary fibrotic and myopathic changes. However, a primary but yet unexplained neck extensor myopathy still remains the alternative possibility and longitudinal studies are necessary to settle this issue. © 2007 Movement Disorder Society
Url:
DOI: 10.1002/mds.21634
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream Istex, to step Corpus: 001451
- to stream Istex, to step Curation: 001451
- to stream Istex, to step Checkpoint: 001639
- to stream PubMed, to step Corpus: 002482
- to stream PubMed, to step Curation: 002482
- to stream PubMed, to step Checkpoint: 002511
- to stream Ncbi, to step Merge: 001E77
- to stream Ncbi, to step Curation: 001E77
- to stream Ncbi, to step Checkpoint: 001E77
- to stream Main, to step Merge: 003A53
- to stream PascalFrancis, to step Corpus: 001364
- to stream PascalFrancis, to step Curation: 001955
- to stream PascalFrancis, to step Checkpoint: 001436
- to stream Main, to step Merge: 004026
- to stream Main, to step Curation: 002B31
Le document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">The phenomenon of disproportionate antecollis in Parkinson's disease and multiple system atrophy</title><author><name sortKey="Van De Warrenburg, Bart P C" sort="Van De Warrenburg, Bart P C" uniqKey="Van De Warrenburg B" first="Bart P. C." last="Van De Warrenburg">Bart P. C. Van De Warrenburg</name></author><author><name sortKey="Cordivari, Carla" sort="Cordivari, Carla" uniqKey="Cordivari C" first="Carla" last="Cordivari">Carla Cordivari</name></author><author><name sortKey="Ryan, Aisling M" sort="Ryan, Aisling M" uniqKey="Ryan A" first="Aisling M." last="Ryan">Aisling M. Ryan</name></author><author><name sortKey="Phadke, Rahul" sort="Phadke, Rahul" uniqKey="Phadke R" first="Rahul" last="Phadke">Rahul Phadke</name></author><author><name sortKey="Holton, Janice L" sort="Holton, Janice L" uniqKey="Holton J" first="Janice L." last="Holton">Janice L. Holton</name></author><author><name sortKey="Bhatia, Kailash P" sort="Bhatia, Kailash P" uniqKey="Bhatia K" first="Kailash P." last="Bhatia">Kailash P. Bhatia</name></author><author><name sortKey="Hanna, Mike G" sort="Hanna, Mike G" uniqKey="Hanna M" first="Mike G." last="Hanna">Mike G. Hanna</name></author><author><name sortKey="Quinn, Niall P" sort="Quinn, Niall P" uniqKey="Quinn N" first="Niall P." last="Quinn">Niall P. Quinn</name></author></titleStmt><publicationStmt><idno type="wicri:source">ISTEX</idno><idno type="RBID">ISTEX:DBC1B6760A42DD4B02A8D2FBD067E41EF7FFCB49</idno><date when="2007" year="2007">2007</date><idno type="doi">10.1002/mds.21634</idno><idno type="url">https://api.istex.fr/document/DBC1B6760A42DD4B02A8D2FBD067E41EF7FFCB49/fulltext/pdf</idno><idno type="wicri:Area/Istex/Corpus">001451</idno><idno type="wicri:Area/Istex/Curation">001451</idno><idno type="wicri:Area/Istex/Checkpoint">001639</idno><idno type="wicri:doubleKey">0885-3185:2007:Van De Warrenburg B:the:phenomenon:of</idno><idno type="wicri:source">PubMed</idno><idno type="RBID">pubmed:17960814</idno><idno type="wicri:Area/PubMed/Corpus">002482</idno><idno type="wicri:Area/PubMed/Curation">002482</idno><idno type="wicri:Area/PubMed/Checkpoint">002511</idno><idno type="wicri:Area/Ncbi/Merge">001E77</idno><idno type="wicri:Area/Ncbi/Curation">001E77</idno><idno type="wicri:Area/Ncbi/Checkpoint">001E77</idno><idno type="wicri:doubleKey">0885-3185:2007:Van De Warrenburg B:the:phenomenon:of</idno><idno type="wicri:Area/Main/Merge">003A53</idno><idno type="wicri:source">INIST</idno><idno type="RBID">Pascal:08-0147019</idno><idno type="wicri:Area/PascalFrancis/Corpus">001364</idno><idno type="wicri:Area/PascalFrancis/Curation">001955</idno><idno type="wicri:Area/PascalFrancis/Checkpoint">001436</idno><idno type="wicri:doubleKey">0885-3185:2007:Van De Warrenburg B:the:phenomenon:of</idno><idno type="wicri:Area/Main/Merge">004026</idno><idno type="wicri:Area/Main/Curation">002B31</idno><idno type="wicri:Area/Main/Exploration">002B31</idno></publicationStmt><sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">The phenomenon of disproportionate antecollis in Parkinson's disease and multiple system atrophy</title><author><name sortKey="Van De Warrenburg, Bart P C" sort="Van De Warrenburg, Bart P C" uniqKey="Van De Warrenburg B" first="Bart P. C." last="Van De Warrenburg">Bart P. C. Van De Warrenburg</name><affiliation wicri:level="3"><country xml:lang="fr">Royaume-Uni</country><wicri:regionArea>Sobell Department of Motor Neuroscience and Movement Disorders, Institute of Neurology, London</wicri:regionArea><placeName><settlement type="city">Londres</settlement><region type="country">Angleterre</region><region type="région" nuts="1">Grand Londres</region></placeName></affiliation><affiliation wicri:level="3"><country xml:lang="fr">Pays-Bas</country><wicri:regionArea>Department of Neurology, Radboud University Nijmegen Medical Centre, Nijmegen</wicri:regionArea><placeName><settlement type="city">Nimègue</settlement><region type="province" nuts="2">Gueldre</region></placeName></affiliation></author><author><name sortKey="Cordivari, Carla" sort="Cordivari, Carla" uniqKey="Cordivari C" first="Carla" last="Cordivari">Carla Cordivari</name><affiliation wicri:level="3"><country xml:lang="fr">Royaume-Uni</country><wicri:regionArea>Department of Neurophysiology, National Hospital of Neurology and Neurosurgery, London</wicri:regionArea><placeName><settlement type="city">Londres</settlement><region type="country">Angleterre</region><region type="région" nuts="1">Grand Londres</region></placeName></affiliation></author><author><name sortKey="Ryan, Aisling M" sort="Ryan, Aisling M" uniqKey="Ryan A" first="Aisling M." last="Ryan">Aisling M. Ryan</name><affiliation wicri:level="3"><country xml:lang="fr">Royaume-Uni</country><wicri:regionArea>Centre for Neuromuscular Disease, National Hospital of Neurology and Neurosurgery, London</wicri:regionArea><placeName><settlement type="city">Londres</settlement><region type="country">Angleterre</region><region type="région" nuts="1">Grand Londres</region></placeName></affiliation></author><author><name sortKey="Phadke, Rahul" sort="Phadke, Rahul" uniqKey="Phadke R" first="Rahul" last="Phadke">Rahul Phadke</name><affiliation wicri:level="3"><country xml:lang="fr">Royaume-Uni</country><wicri:regionArea>Division of Neuropathology, Institute of Neurology, London</wicri:regionArea><placeName><settlement type="city">Londres</settlement><region type="country">Angleterre</region><region type="région" nuts="1">Grand Londres</region></placeName></affiliation></author><author><name sortKey="Holton, Janice L" sort="Holton, Janice L" uniqKey="Holton J" first="Janice L." last="Holton">Janice L. Holton</name><affiliation wicri:level="3"><country xml:lang="fr">Royaume-Uni</country><wicri:regionArea>Division of Neuropathology, Institute of Neurology, London</wicri:regionArea><placeName><settlement type="city">Londres</settlement><region type="country">Angleterre</region><region type="région" nuts="1">Grand Londres</region></placeName></affiliation></author><author><name sortKey="Bhatia, Kailash P" sort="Bhatia, Kailash P" uniqKey="Bhatia K" first="Kailash P." last="Bhatia">Kailash P. Bhatia</name><affiliation wicri:level="3"><country xml:lang="fr">Royaume-Uni</country><wicri:regionArea>Sobell Department of Motor Neuroscience and Movement Disorders, Institute of Neurology, London</wicri:regionArea><placeName><settlement type="city">Londres</settlement><region type="country">Angleterre</region><region type="région" nuts="1">Grand Londres</region></placeName></affiliation></author><author><name sortKey="Hanna, Mike G" sort="Hanna, Mike G" uniqKey="Hanna M" first="Mike G." last="Hanna">Mike G. Hanna</name><affiliation wicri:level="3"><country xml:lang="fr">Royaume-Uni</country><wicri:regionArea>Department of Molecular Neuroscience, Institute of Neurology, London</wicri:regionArea><placeName><settlement type="city">Londres</settlement><region type="country">Angleterre</region><region type="région" nuts="1">Grand Londres</region></placeName></affiliation></author><author><name sortKey="Quinn, Niall P" sort="Quinn, Niall P" uniqKey="Quinn N" first="Niall P." last="Quinn">Niall P. Quinn</name><affiliation wicri:level="3"><country xml:lang="fr">Royaume-Uni</country><wicri:regionArea>Sobell Department of Motor Neuroscience and Movement Disorders, Institute of Neurology, London</wicri:regionArea><placeName><settlement type="city">Londres</settlement><region type="country">Angleterre</region><region type="région" nuts="1">Grand Londres</region></placeName></affiliation></author></analytic><monogr></monogr><series><title level="j">Movement Disorders</title><title level="j" type="abbrev">Mov. Disord.</title><idno type="ISSN">0885-3185</idno><idno type="eISSN">1531-8257</idno><imprint><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><pubPlace>Hoboken</pubPlace><date type="published" when="2007-12-15">2007-12-15</date><biblScope unit="vol">22</biblScope><biblScope unit="issue">16</biblScope><biblScope unit="page" from="2325">2325</biblScope><biblScope unit="page" to="2331">2331</biblScope></imprint><idno type="ISSN">0885-3185</idno></series><idno type="istex">DBC1B6760A42DD4B02A8D2FBD067E41EF7FFCB49</idno><idno type="DOI">10.1002/mds.21634</idno><idno type="ArticleID">MDS21634</idno></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0885-3185</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aged</term><term>Antiparkinson Agents (therapeutic use)</term><term>Botulinum Toxins, Type A (therapeutic use)</term><term>Electromyography</term><term>Electrophysiology</term><term>Female</term><term>Fibrosis (pathology)</term><term>Head</term><term>Humans</term><term>Levodopa (therapeutic use)</term><term>Male</term><term>Middle Aged</term><term>Movement (physiology)</term><term>Multiple System Atrophy (drug therapy)</term><term>Multiple System Atrophy (pathology)</term><term>Multiple System Atrophy (physiopathology)</term><term>Multiple system atrophy</term><term>Muscle, Skeletal (pathology)</term><term>Muscle, Skeletal (physiopathology)</term><term>Myopathy</term><term>Neck</term><term>Nervous system diseases</term><term>Neuromuscular Agents (therapeutic use)</term><term>Parkinson Disease (drug therapy)</term><term>Parkinson Disease (pathology)</term><term>Parkinson Disease (physiopathology)</term><term>Parkinson disease</term><term>Parkinson's disease</term><term>antecollis</term><term>dropped head</term><term>multiple system atrophy</term><term>myopathy</term></keywords><keywords scheme="MESH" type="chemical" qualifier="therapeutic use" xml:lang="en"><term>Antiparkinson Agents</term><term>Botulinum Toxins, Type A</term><term>Levodopa</term><term>Neuromuscular Agents</term></keywords><keywords scheme="MESH" qualifier="drug therapy" xml:lang="en"><term>Multiple System Atrophy</term><term>Parkinson Disease</term></keywords><keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Fibrosis</term><term>Multiple System Atrophy</term><term>Muscle, Skeletal</term><term>Parkinson Disease</term></keywords><keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Movement</term></keywords><keywords scheme="MESH" qualifier="physiopathology" xml:lang="en"><term>Multiple System Atrophy</term><term>Muscle, Skeletal</term><term>Parkinson Disease</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Aged</term><term>Electromyography</term><term>Electrophysiology</term><term>Female</term><term>Head</term><term>Humans</term><term>Male</term><term>Middle Aged</term><term>Neck</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Atrophie multisystématisée</term><term>Maladie de Parkinson</term><term>Myopathie</term><term>Pathologie du système nerveux</term><term>Tête</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">We sought to explore the phenomenon of disproportionate antecollis in multiple system atrophy (MSA) and Parkinson's disease (PD). The etiology is much debated and the main issue is whether it represents a primary myopathy or is secondary to the underlying motor disorder. The clinical, electrophysiological, and biopsy data of MSA or PD patients with antecollis were reviewed. We reviewed 16 patients (7 MSA and 9 PD) who developed antecollis during the course of their disease. The interval between onset of motor symptoms and of antecollis was shorter in the MSA group (4.6 ± 1.7 years vs. 10.5 ± 7.0 years). In 6 patients, the antecollis developed subacutely, and in 2 the abnormal neck flexion was initially an off‐period phenomenon. Two additional patients also showed some dopa‐responsiveness. Clinically, the antecollis was characterized by a forward flexion and anterior shift of the neck, with prominent cervical paraspinal and levator scapulae muscles, usually without weakness of residual neck extension. Electromyography of cervical paraspinal muscles showed mixed myopathic, normal, and neurogenic units, without early recruitment. Cervical paraspinal muscle biopsy in 2 patients disclosed fibrosis and nonspecific myopathic changes. We suggest that, in the context of MSA or PD, the initiating event in antecollis could be a disproportionately increased tone in anterior neck muscles that leads to secondary fibrotic and myopathic changes. However, a primary but yet unexplained neck extensor myopathy still remains the alternative possibility and longitudinal studies are necessary to settle this issue. © 2007 Movement Disorder Society</div></front></TEI><affiliations><list><country><li>Pays-Bas</li><li>Royaume-Uni</li></country><region><li>Angleterre</li><li>Grand Londres</li><li>Gueldre</li></region><settlement><li>Londres</li><li>Nimègue</li></settlement></list><tree><country name="Royaume-Uni"><region name="Angleterre"><name sortKey="Van De Warrenburg, Bart P C" sort="Van De Warrenburg, Bart P C" uniqKey="Van De Warrenburg B" first="Bart P. C." last="Van De Warrenburg">Bart P. C. Van De Warrenburg</name></region><name sortKey="Bhatia, Kailash P" sort="Bhatia, Kailash P" uniqKey="Bhatia K" first="Kailash P." last="Bhatia">Kailash P. Bhatia</name><name sortKey="Cordivari, Carla" sort="Cordivari, Carla" uniqKey="Cordivari C" first="Carla" last="Cordivari">Carla Cordivari</name><name sortKey="Hanna, Mike G" sort="Hanna, Mike G" uniqKey="Hanna M" first="Mike G." last="Hanna">Mike G. Hanna</name><name sortKey="Holton, Janice L" sort="Holton, Janice L" uniqKey="Holton J" first="Janice L." last="Holton">Janice L. Holton</name><name sortKey="Phadke, Rahul" sort="Phadke, Rahul" uniqKey="Phadke R" first="Rahul" last="Phadke">Rahul Phadke</name><name sortKey="Quinn, Niall P" sort="Quinn, Niall P" uniqKey="Quinn N" first="Niall P." last="Quinn">Niall P. Quinn</name><name sortKey="Ryan, Aisling M" sort="Ryan, Aisling M" uniqKey="Ryan A" first="Aisling M." last="Ryan">Aisling M. Ryan</name></country><country name="Pays-Bas"><region name="Gueldre"><name sortKey="Van De Warrenburg, Bart P C" sort="Van De Warrenburg, Bart P C" uniqKey="Van De Warrenburg B" first="Bart P. C." last="Van De Warrenburg">Bart P. C. Van De Warrenburg</name></region></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Santé/explor/MovDisordV3/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 002B31 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 002B31 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien
|wiki= Wicri/Santé
|area= MovDisordV3
|flux= Main
|étape= Exploration
|type= RBID
|clé= ISTEX:DBC1B6760A42DD4B02A8D2FBD067E41EF7FFCB49
|texte= The phenomenon of disproportionate antecollis in Parkinson's disease and multiple system atrophy
}}
| This area was generated with Dilib version V0.6.23. |  |