A Case Series of Unilateral Peripheral Neuropathy
A unilateral, slowly progressive peripheral neuropathy is a rare phenomenon, and we propose the cause of this unusual phenotype to be due to a mosaic or chimeric form of Charcot-Marie-Tooth disease (CMT).
Authors
- Françoise Bouhour (ORCID: https://orcid.org/0000-0002-4005-1537)
- Alexander Martin Rossor (ORCID: https://orcid.org/0000-0003-4648-2896)
- Mary M. Reilly (ORCID: https://orcid.org/0000-0003-0686-905X)
- Caroline Kramarz (ORCID: https://orcid.org/0009-0005-2480-3590)
- Christophe Vial (ORCID: https://orcid.org/0000-0002-9503-1605)
- Jan Coebergh (ORCID: https://orcid.org/0000-0003-2357-6988)
- Philippe Latour (ORCID: https://orcid.org/0000-0002-2370-1331)
- Thierry Maisonobe (ORCID: https://orcid.org/0000-0002-9758-0085)
- Christophe Vandendries (ORCID: https://orcid.org/0000-0003-3587-3808)
- Marion Masingue (ORCID: https://orcid.org/0000-0002-4898-709X)
- Tanya Stojkovic
- Julian Blake
Institutions
- National Health Service (GB)
- Norfolk and Norwich University Hospital (GB)
- St George’s University Hospitals NHS Foundation Trust (GB)
- Assistance Publique – Hôpitaux de Paris (FR)
- Hospices Civils de Lyon (FR)
- Institut de Myologie (FR)
- National Hospital for Neurology and Neurosurgery (GB)
- University College London (GB)
Publication Details
- Journal
- Journal of the Peripheral Nervous System
- Published
- 2025-05-26
- DOI
- https://doi.org/10.1111/jns.70033
- Primary Topic
- Hereditary Neurological Disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.00