Skip to main content
Advertisement
  • Neurology.org
  • Journals
    • Neurology
    • Clinical Practice
    • Education
    • Genetics
    • Neuroimmunology & Neuroinflammation
  • Online Sections
    • Neurology Video Journal Club
    • Diversity, Equity, & Inclusion (DEI)
    • Neurology: Clinical Practice Accelerator
    • Practice Buzz
    • Practice Current
    • Residents & Fellows
    • Without Borders
  • Collections
    • COVID-19
    • Disputes & Debates
    • Health Disparities
    • Infographics
    • Neurology Future Forecasting Series
    • Null Hypothesis
    • Patient Pages
    • Topics A-Z
    • Translations
    • UDDA Revision Series
  • Podcast
  • CME
  • About
    • About the Journals
    • Contact Us
    • Editorial Board
  • Authors
    • Submit Manuscript
    • Author Center

Advanced Search

Main menu

  • Neurology.org
  • Journals
    • Neurology
    • Clinical Practice
    • Education
    • Genetics
    • Neuroimmunology & Neuroinflammation
  • Online Sections
    • Neurology Video Journal Club
    • Diversity, Equity, & Inclusion (DEI)
    • Neurology: Clinical Practice Accelerator
    • Practice Buzz
    • Practice Current
    • Residents & Fellows
    • Without Borders
  • Collections
    • COVID-19
    • Disputes & Debates
    • Health Disparities
    • Infographics
    • Neurology Future Forecasting Series
    • Null Hypothesis
    • Patient Pages
    • Topics A-Z
    • Translations
    • UDDA Revision Series
  • Podcast
  • CME
  • About
    • About the Journals
    • Contact Us
    • Editorial Board
  • Authors
    • Submit Manuscript
    • Author Center
  • Home
  • Latest Articles
  • Current Issue
  • Past Issues
  • Neurology Video Journal Club
  • Residents & Fellows

User menu

  • Subscribe
  • My Alerts
  • Log in

Search

  • Advanced search
Neurology
Home
The most widely read and highly cited peer-reviewed neurology journal
  • Subscribe
  • My Alerts
  • Log in
Site Logo
  • Home
  • Latest Articles
  • Current Issue
  • Past Issues
  • Neurology Video Journal Club
  • Residents & Fellows

Share

February 24, 2015; 84 (8) Video NeuroImages

Congenital mirror movements

From piano player to opera singer

Aurélie Méneret, Quentin Welniarz, Oriane Trouillard, Emmanuel Roze
First published February 23, 2015, DOI: https://doi.org/10.1212/WNL.0000000000001290
Aurélie Méneret
From Inserm (A.M., Q.W., O.T., E.R.), U 1127; CNRS (A.M., Q.W., O.T., E.R.), UMR 7225; Sorbonne Universités (A.M., Q.W., O.T., E.R.), UPMC Univ Paris 06, UMR S 1127; Institut du Cerveau et de la Moelle épinière (A.M., Q.W., O.T., E.R.), ICM; AP-HP (A.M., E.R.), Département de Neurologie, Hôpital de la Pitié Salpêtrière; and Neuroscience Paris Seine (Q.W.), CNRS UMR8246, Inserm U1130, Paris, France.
MD
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Quentin Welniarz
From Inserm (A.M., Q.W., O.T., E.R.), U 1127; CNRS (A.M., Q.W., O.T., E.R.), UMR 7225; Sorbonne Universités (A.M., Q.W., O.T., E.R.), UPMC Univ Paris 06, UMR S 1127; Institut du Cerveau et de la Moelle épinière (A.M., Q.W., O.T., E.R.), ICM; AP-HP (A.M., E.R.), Département de Neurologie, Hôpital de la Pitié Salpêtrière; and Neuroscience Paris Seine (Q.W.), CNRS UMR8246, Inserm U1130, Paris, France.
MS
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Oriane Trouillard
From Inserm (A.M., Q.W., O.T., E.R.), U 1127; CNRS (A.M., Q.W., O.T., E.R.), UMR 7225; Sorbonne Universités (A.M., Q.W., O.T., E.R.), UPMC Univ Paris 06, UMR S 1127; Institut du Cerveau et de la Moelle épinière (A.M., Q.W., O.T., E.R.), ICM; AP-HP (A.M., E.R.), Département de Neurologie, Hôpital de la Pitié Salpêtrière; and Neuroscience Paris Seine (Q.W.), CNRS UMR8246, Inserm U1130, Paris, France.
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Emmanuel Roze
From Inserm (A.M., Q.W., O.T., E.R.), U 1127; CNRS (A.M., Q.W., O.T., E.R.), UMR 7225; Sorbonne Universités (A.M., Q.W., O.T., E.R.), UPMC Univ Paris 06, UMR S 1127; Institut du Cerveau et de la Moelle épinière (A.M., Q.W., O.T., E.R.), ICM; AP-HP (A.M., E.R.), Département de Neurologie, Hôpital de la Pitié Salpêtrière; and Neuroscience Paris Seine (Q.W.), CNRS UMR8246, Inserm U1130, Paris, France.
MD, PhD
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Full PDF
Citation
Congenital mirror movements
From piano player to opera singer
Aurélie Méneret, Quentin Welniarz, Oriane Trouillard, Emmanuel Roze
Neurology Feb 2015, 84 (8) 860; DOI: 10.1212/WNL.0000000000001290

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero
Permissions

Make Comment

See Comments

Downloads
729

Share

  • Article
  • Figures & Data
  • Info & Disclosures
Loading

Congenital mirror movements (CMM) disorder is characterized by involuntary movements of one side of the body that accompany and mirror intentional movements on the opposite side (OMIM #157600).1 CMM mostly involve the hands, and affected subjects are unable to perform pure unimanual movements or skilled dissociated movements of the 2 hands. We show a 33-year-old patient with CMM with no abnormality in DCC or RAD51, the known culprit genes (video on the Neurology® Web site at Neurology.org).2 He had always dreamed of becoming a piano player but was unable to play properly with both hands despite intensive training. He became an opera singer instead.

Footnotes

  • Supplemental data at Neurology.org

  • Author contributions: Aurélie Méneret: drafting/revising the manuscript, analysis or interpretation of data, accepts responsibility for conduct of research and final approval. Quentin Welniarz: analysis or interpretation of data, accepts responsibility for conduct of research and final approval, acquisition of data. Oriane Trouillard: analysis or interpretation of data, accepts responsibility for conduct of research and final approval. Emmanuel Roze: drafting/revising the manuscript, study concept or design, analysis or interpretation of data, accepts responsibility for conduct of research and final approval, study supervision.

  • Study funding: No targeted funding reported.

  • Disclosure: A. Méneret received a research grant from AP-HP and received travel funding from ANAINF, JNLF, and the European Federation of the Neurological Societies. Q. Welniarz and O. Trouillard report no disclosures relevant to the manuscript. E. Roze is the recipient of a grant “poste d'accueil” AP-HP/CNRS. He received research support from INSERM (COSSEC), AP-HP (DRC-PHRC), Fondation pour la Recherche sur le Cerveau (FRC), the Dystonia Coalition (Pilot project), Ipsen, Merz-Pharma, Novartis, Teva, Lundbeck, and Orkyn; served on scientific advisory boards for Orkyn, Ipsen, and Merz-Pharma; received speech honorarium from Novartis, Teva, and Orkyn; and received travel funding from Teva, Novartis, the Dystonia Coalition, the Movement Disorders Society, the World Federation of Neurology Association of Parkinsonism and Related Disorders, and International Federation of Clinical Neurophysiology. Go to Neurology.org for full disclosures.

  • © 2015 American Academy of Neurology

References

  1. 1.↵
    1. Gallea C,
    2. Popa T,
    3. Billot S,
    4. Meneret A,
    5. Depienne C,
    6. Roze E
    . Congenital mirror movements: a clue to understanding bimanual motor control. J Neurol 2011;258:1911–1919.
    OpenUrlCrossRefPubMed
  2. 2.↵
    1. Meneret A,
    2. Depienne C,
    3. Riant F,
    4. et al
    . Congenital mirror movements: mutational analysis of RAD51 and DCC in 26 cases. Neurology 2014;82:1999–2002.
    OpenUrlAbstract/FREE Full Text
View Abstract

Letters: Rapid online correspondence

No comments have been published for this article.
Comment

REQUIREMENTS

You must ensure that your Disclosures have been updated within the previous six months. Please go to our Submission Site to add or update your Disclosure information.

Your co-authors must send a completed Publishing Agreement Form to Neurology Staff (not necessary for the lead/corresponding author as the form below will suffice) before you upload your comment.

If you are responding to a comment that was written about an article you originally authored:
You (and co-authors) do not need to fill out forms or check disclosures as author forms are still valid
and apply to letter.

Submission specifications:

  • Submissions must be < 200 words with < 5 references. Reference 1 must be the article on which you are commenting.
  • Submissions should not have more than 5 authors. (Exception: original author replies can include all original authors of the article)
  • Submit only on articles published within 6 months of issue date.
  • Do not be redundant. Read any comments already posted on the article prior to submission.
  • Submitted comments are subject to editing and editor review prior to posting.

More guidelines and information on Disputes & Debates

Compose Comment

More information about text formats

Plain text

  • No HTML tags allowed.
  • Web page addresses and e-mail addresses turn into links automatically.
  • Lines and paragraphs break automatically.
Author Information
NOTE: The first author must also be the corresponding author of the comment.
First or given name, e.g. 'Peter'.
Your last, or family, name, e.g. 'MacMoody'.
Your email address, e.g. [email protected]
Your role and/or occupation, e.g. 'Orthopedic Surgeon'.
Your organization or institution (if applicable), e.g. 'Royal Free Hospital'.
Publishing Agreement
NOTE: All authors, besides the first/corresponding author, must complete a separate Publishing Agreement Form and provide via email to the editorial office before comments can be posted.
CAPTCHA
This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.

Vertical Tabs

You May Also be Interested in

Back to top
  • Article
    • Footnotes
    • References
  • Figures & Data
  • Info & Disclosures
Advertisement

Hastening the Diagnosis of Amyotrophic Lateral Sclerosis

Dr. Brian Callaghan and Dr. Kellen Quigg

► Watch

Topics Discussed

  • All Genetics
  • Motor Control

Alert Me

  • Alert me when eletters are published

Recommended articles

  • Article
    Congenital mirror movements
    Mutational analysis of RAD51 and DCC in 26 cases

    Aurélie Méneret, Christel Depienne, Florence Riant et al.
    Neurology, May 07, 2014
  • Article
    Heterozygous variants in DCC
    Beyond congenital mirror movements
    Sebastian Thams, Mominul Islam, Marie Lindefeldt et al.
    Neurology: Genetics, October 20, 2020
  • Clinical/Scientific Notes
    FAMILIAL CONGENITAL MIRROR MOVEMENTS: REPORT OF A LARGE 4-GENERATION FAMILY
    M. Srour, M. Philibert, M. -H. Dion et al.
    Neurology, August 31, 2009
  • Articles
    A novel DCC mutation and genetic heterogeneity in congenital mirror movements
    C. Depienne, M. Cincotta, S. Billot et al.
    Neurology, January 17, 2011
Neurology: 101 (22)

Articles

  • Ahead of Print
  • Current Issue
  • Past Issues
  • Popular Articles
  • Translations

About

  • About the Journals
  • Ethics Policies
  • Editors & Editorial Board
  • Contact Us
  • Advertise

Submit

  • Author Center
  • Submit a Manuscript
  • Information for Reviewers
  • AAN Guidelines
  • Permissions

Subscribers

  • Subscribe
  • Activate a Subscription
  • Sign up for eAlerts
  • RSS Feed
Site Logo
  • Visit neurology Template on Facebook
  • Follow neurology Template on Twitter
  • Visit Neurology on YouTube
  • Neurology
  • Neurology: Clinical Practice
  • Neurology: Education
  • Neurology: Genetics
  • Neurology: Neuroimmunology & Neuroinflammation
  • AAN.com
  • Continuum
  • Brain & Life
  • Neurology Today

Wolters Kluwer Logo

Neurology | Print ISSN:0028-3878
Online ISSN:1526-632X

© 2023 American Academy of Neurology

  • Privacy Policy
  • Feedback
  • Advertise