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Presence of both anti-contactin 1 and anti-neurofascin 140 antibodies in a case of chronic inflammatory demyelinating polyneuropathy

Chronic inflammatory demyelinating polyneuropathy (CIDP) is an acquired disorder of peripheral nerves and nerve roots. Its cause is unknown, but recently antibodies to nodal and paranodal proteins have been discovered in a small subset of CIDP patients. These contactin and neurofascin-related immune...

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Autores principales: Lin, Hsin-Pin, Ho, Kwo Wei David, Chuquilin, Miguel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6275845/
https://www.ncbi.nlm.nih.gov/pubmed/30547099
http://dx.doi.org/10.1016/j.ensci.2018.11.016
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author Lin, Hsin-Pin
Ho, Kwo Wei David
Chuquilin, Miguel
author_facet Lin, Hsin-Pin
Ho, Kwo Wei David
Chuquilin, Miguel
author_sort Lin, Hsin-Pin
collection PubMed
description Chronic inflammatory demyelinating polyneuropathy (CIDP) is an acquired disorder of peripheral nerves and nerve roots. Its cause is unknown, but recently antibodies to nodal and paranodal proteins have been discovered in a small subset of CIDP patients. These contactin and neurofascin-related immune-mediated neuropathies are thought to be variants of CIDP and often respond suboptimally to standard therapy. Here, we report a patient with both anti-contactin 1 and anti-neurofascin 140 antibodies whose presentation resembled phenotypes of both CIDP variants.
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spelling pubmed-62758452018-12-13 Presence of both anti-contactin 1 and anti-neurofascin 140 antibodies in a case of chronic inflammatory demyelinating polyneuropathy Lin, Hsin-Pin Ho, Kwo Wei David Chuquilin, Miguel eNeurologicalSci Case Report Chronic inflammatory demyelinating polyneuropathy (CIDP) is an acquired disorder of peripheral nerves and nerve roots. Its cause is unknown, but recently antibodies to nodal and paranodal proteins have been discovered in a small subset of CIDP patients. These contactin and neurofascin-related immune-mediated neuropathies are thought to be variants of CIDP and often respond suboptimally to standard therapy. Here, we report a patient with both anti-contactin 1 and anti-neurofascin 140 antibodies whose presentation resembled phenotypes of both CIDP variants. Elsevier 2018-11-22 /pmc/articles/PMC6275845/ /pubmed/30547099 http://dx.doi.org/10.1016/j.ensci.2018.11.016 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Lin, Hsin-Pin
Ho, Kwo Wei David
Chuquilin, Miguel
Presence of both anti-contactin 1 and anti-neurofascin 140 antibodies in a case of chronic inflammatory demyelinating polyneuropathy
title Presence of both anti-contactin 1 and anti-neurofascin 140 antibodies in a case of chronic inflammatory demyelinating polyneuropathy
title_full Presence of both anti-contactin 1 and anti-neurofascin 140 antibodies in a case of chronic inflammatory demyelinating polyneuropathy
title_fullStr Presence of both anti-contactin 1 and anti-neurofascin 140 antibodies in a case of chronic inflammatory demyelinating polyneuropathy
title_full_unstemmed Presence of both anti-contactin 1 and anti-neurofascin 140 antibodies in a case of chronic inflammatory demyelinating polyneuropathy
title_short Presence of both anti-contactin 1 and anti-neurofascin 140 antibodies in a case of chronic inflammatory demyelinating polyneuropathy
title_sort presence of both anti-contactin 1 and anti-neurofascin 140 antibodies in a case of chronic inflammatory demyelinating polyneuropathy
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6275845/
https://www.ncbi.nlm.nih.gov/pubmed/30547099
http://dx.doi.org/10.1016/j.ensci.2018.11.016
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