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Severe distinct dysautonomia in RFC1 ‐related disease associated with Parkinsonism
Biallelic repeat expansions in replication factor C subunit 1 (RFC1) have recently been found to cause cerebellar ataxia, neuropathy and vestibular areflexia syndrome (CANVAS). Additional features that have been described include Parkinsonism and a multiple system atrophy (MSA)‐like syndrome. CANVAS...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wiley Periodicals, Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10092280/ https://www.ncbi.nlm.nih.gov/pubmed/36177974 http://dx.doi.org/10.1111/jns.12515 |
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author | Record, Christopher J. Alsukhni, Rana Alnasser Curro, Riccardo Kaski, Diego Rubin, John S. Morris, Huw R. Cortese, Andrea Iodice, Valeria Reilly, Mary M. |
author_facet | Record, Christopher J. Alsukhni, Rana Alnasser Curro, Riccardo Kaski, Diego Rubin, John S. Morris, Huw R. Cortese, Andrea Iodice, Valeria Reilly, Mary M. |
author_sort | Record, Christopher J. |
collection | PubMed |
description | Biallelic repeat expansions in replication factor C subunit 1 (RFC1) have recently been found to cause cerebellar ataxia, neuropathy and vestibular areflexia syndrome (CANVAS). Additional features that have been described include Parkinsonism and a multiple system atrophy (MSA)‐like syndrome. CANVAS can include features of dysautonomia, but they are much milder than typically seen in MSA. We report a detailed autonomic phenotype of multisystem RFC1‐related disease presenting initially as CANVAS. Our patient presented aged 61 with a sensory ataxic neuropathy who rapidly developed widespread autonomic failure and Parkinsonism. The autonomic profile was of a mixed pre‐ and post‐ganglionic syndrome with progressive involvement of sympathetic and parasympathetic cardiovascular and sudomotor function. The Parkinsonism did not respond to levodopa. We present a patient with CANVAS and biallelic RFC1 expansions who developed Parkinsonism with severe autonomic involvement similar to that seen in classical MSA. The link between MSA and CANVAS remains uncertain. |
format | Online Article Text |
id | pubmed-10092280 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Wiley Periodicals, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100922802023-04-13 Severe distinct dysautonomia in RFC1 ‐related disease associated with Parkinsonism Record, Christopher J. Alsukhni, Rana Alnasser Curro, Riccardo Kaski, Diego Rubin, John S. Morris, Huw R. Cortese, Andrea Iodice, Valeria Reilly, Mary M. J Peripher Nerv Syst Case Reports Biallelic repeat expansions in replication factor C subunit 1 (RFC1) have recently been found to cause cerebellar ataxia, neuropathy and vestibular areflexia syndrome (CANVAS). Additional features that have been described include Parkinsonism and a multiple system atrophy (MSA)‐like syndrome. CANVAS can include features of dysautonomia, but they are much milder than typically seen in MSA. We report a detailed autonomic phenotype of multisystem RFC1‐related disease presenting initially as CANVAS. Our patient presented aged 61 with a sensory ataxic neuropathy who rapidly developed widespread autonomic failure and Parkinsonism. The autonomic profile was of a mixed pre‐ and post‐ganglionic syndrome with progressive involvement of sympathetic and parasympathetic cardiovascular and sudomotor function. The Parkinsonism did not respond to levodopa. We present a patient with CANVAS and biallelic RFC1 expansions who developed Parkinsonism with severe autonomic involvement similar to that seen in classical MSA. The link between MSA and CANVAS remains uncertain. Wiley Periodicals, Inc. 2022-10-07 2022-12 /pmc/articles/PMC10092280/ /pubmed/36177974 http://dx.doi.org/10.1111/jns.12515 Text en © 2022 The Authors. Journal of the Peripheral Nervous System published by Wiley Periodicals LLC on behalf of Peripheral Nerve Society. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Reports Record, Christopher J. Alsukhni, Rana Alnasser Curro, Riccardo Kaski, Diego Rubin, John S. Morris, Huw R. Cortese, Andrea Iodice, Valeria Reilly, Mary M. Severe distinct dysautonomia in RFC1 ‐related disease associated with Parkinsonism |
title | Severe distinct dysautonomia in
RFC1
‐related disease associated with Parkinsonism |
title_full | Severe distinct dysautonomia in
RFC1
‐related disease associated with Parkinsonism |
title_fullStr | Severe distinct dysautonomia in
RFC1
‐related disease associated with Parkinsonism |
title_full_unstemmed | Severe distinct dysautonomia in
RFC1
‐related disease associated with Parkinsonism |
title_short | Severe distinct dysautonomia in
RFC1
‐related disease associated with Parkinsonism |
title_sort | severe distinct dysautonomia in
rfc1
‐related disease associated with parkinsonism |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10092280/ https://www.ncbi.nlm.nih.gov/pubmed/36177974 http://dx.doi.org/10.1111/jns.12515 |
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