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Quang Tuan Rémy Nguyen1,2,3*
Juan Dario Ortigoza Escobar4,5Jean-Marc Burgunder5,6Caterina Mariotti5,7Carsten Saft5,8Lena Elisabeth Hjermind5,9Katia Youssov1,2G. Bernhard Landwehrmeyer5,10Anne-Catherine Bachoud-Lévi1,3,5*- 1AP-HP, Hôpital Henri Mondor-Albert Chenevier, Centre National de Référence Maladie de Huntington, Service de Neurologie, Créteil, France
- 2Univ Paris Est Creteil, INSERM U955, Institut Mondor de Recherche Biomédicale, Laboratoire de Neuropsychologie Interventionnelle, Creteil, France
- 3Département d'Etudes Cognitives, École normale supérieure, PSL University, Paris, France
- 4Movement Disorders Unit, Institut de Recerca Sant Joan de Déu, CIBERER-ISCIII, Barcelona, Spain
- 5European Reference Network for Rare Neurological Diseases (ERN-RND), Tübingen, Germany
- 6Siloah and Department of Neurology, Department of Clinical Research, Swiss Huntington's Disease Centre, University of Bern, Bern, Switzerland
- 7Unit of Genetics of Neurodegenerative and Metabolic Diseases, Carlo Besta Neurological Institute IRCCS Foundation, Milan, Italy
- 8Department of Neurology, Huntington Center North Rhine-Westphalia, Ruhr-University, St. Josef-Hospital, Bochum, Germany
- 9Department of Neurology, Rigshospitalet, Danish Dementia Research Centre, Clinic of Neurogenetics, Copenhagen University Hospital, Copenhagen, Denmark
- 10Department of Neurology, University of Ulm, Ulm, Germany
A Corrigendum on
Combining Literature Review With a Ground Truth Approach for Diagnosing Huntington's Disease Phenocopy
by Nguyen, Q. T. R., Ortigoza Escobar, J. D., Burgunder, J.-M., Mariotti, C., Saft, C., Hjermind, L. E., Youssov, K., Landwehrmeyer, G. B., and Bachoud-Lévi, A.-C. (2022). Front. Neurol. 13:817753. doi: 10.3389/fneur.2022.817753
In the original article, there was a mistake in Figure 2 and Figure 3 as published. The figures were swapped incorrectly.
FIGURE 2
Figure 2. Classification of the paraclinical tests. 1st-line: red, 2nd-line: blue, 3rd-line: green. The results of the clustering algorithms are summed in the left columns (results in % of runs of the algorithms). Absolute numbers of votes are reported in the middle columns as “Absolute vote data.” The majority vote (>50% of 25 votes) is highlighted in yellow. Literature results are summarized in the right columns. McLeod: exclusion of the McLeod Kell phenotype by a blood bank (weak Kell antigens and, if available, no reaction with anti-Kx). Ch.acanthocytosis: Western blot for chorein protein.
FIGURE 3
Figure 3. Proposition of a strategy to diagnose HD phenocopy. Ab, Antibodies.
The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.
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Keywords: Huntington's disease, chorea, phenocopy, diagnosis, differential diagnosis, guidelines, daily clinical practice
Citation: Nguyen QTR, Ortigoza Escobar JD, Burgunder J-M, Mariotti C, Saft C, Hjermind LE, Youssov K, Landwehrmeyer GB and Bachoud-Lévi A-C (2022) Corrigendum: Combining Literature Review With a Ground Truth Approach for Diagnosing Huntington's Disease Phenocopy. Front. Neurol. 13:891800. doi: 10.3389/fneur.2022.891800
Received: 08 March 2022; Accepted: 09 March 2022;
Published: 30 March 2022.
Approved by:
Frontiers Editorial Office, Frontiers Media SA, SwitzerlandCopyright © 2022 Nguyen, Ortigoza Escobar, Burgunder, Mariotti, Saft, Hjermind, Youssov, Landwehrmeyer and Bachoud-Lévi. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Quang Tuan Rémy Nguyen, cXVhbmd0dWFuLm5ndXllbkBhcGhwLmZy; Anne-Catherine Bachoud-Lévi, YW5uZS1jYXRoZXJpbmUuYmFjaG91ZC1sZXZpQGFwaHAuZnI=