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Tongue atrophy and fasciculations in transthyretin familial amyloid neuropathy: An ALS mimicker

OBJECTIVE: Macroglossia is a well-known feature of amyloidosis; however, tongue atrophy and fasciculations are rarely seen and can lead to the misdiagnosis of amyotrophic lateral sclerosis (ALS). METHODS: We identified 2 unrelated patients with atypical features of tongue atrophy and fasciculations...

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Autores principales: Goyal, Namita A., Mozaffar, Tahseen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4807904/
https://www.ncbi.nlm.nih.gov/pubmed/27066555
http://dx.doi.org/10.1212/NXG.0000000000000018
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author Goyal, Namita A.
Mozaffar, Tahseen
author_facet Goyal, Namita A.
Mozaffar, Tahseen
author_sort Goyal, Namita A.
collection PubMed
description OBJECTIVE: Macroglossia is a well-known feature of amyloidosis; however, tongue atrophy and fasciculations are rarely seen and can lead to the misdiagnosis of amyotrophic lateral sclerosis (ALS). METHODS: We identified 2 unrelated patients with atypical features of tongue atrophy and fasciculations in the setting of a severe neuropathy. RESULTS: Both patients were confirmed to have transthyretin-related familial amyloid polyneuropathy (TTR-FAP) by genetic testing. CONCLUSIONS: TTR-FAP should be considered as a possible mimicker of ALS when tongue atrophy and fasciculations are seen in the setting of a severely progressive polyneuropathy. Other atypical mimickers of ALS include polyglucosan body disease, hexosaminidase A deficiency, multisystem proteinopathy, and Allgrove syndrome.
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spelling pubmed-48079042016-04-08 Tongue atrophy and fasciculations in transthyretin familial amyloid neuropathy: An ALS mimicker Goyal, Namita A. Mozaffar, Tahseen Neurol Genet Article OBJECTIVE: Macroglossia is a well-known feature of amyloidosis; however, tongue atrophy and fasciculations are rarely seen and can lead to the misdiagnosis of amyotrophic lateral sclerosis (ALS). METHODS: We identified 2 unrelated patients with atypical features of tongue atrophy and fasciculations in the setting of a severe neuropathy. RESULTS: Both patients were confirmed to have transthyretin-related familial amyloid polyneuropathy (TTR-FAP) by genetic testing. CONCLUSIONS: TTR-FAP should be considered as a possible mimicker of ALS when tongue atrophy and fasciculations are seen in the setting of a severely progressive polyneuropathy. Other atypical mimickers of ALS include polyglucosan body disease, hexosaminidase A deficiency, multisystem proteinopathy, and Allgrove syndrome. Wolters Kluwer 2015-07-30 /pmc/articles/PMC4807904/ /pubmed/27066555 http://dx.doi.org/10.1212/NXG.0000000000000018 Text en © 2015 American Academy of Neurology This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially.
spellingShingle Article
Goyal, Namita A.
Mozaffar, Tahseen
Tongue atrophy and fasciculations in transthyretin familial amyloid neuropathy: An ALS mimicker
title Tongue atrophy and fasciculations in transthyretin familial amyloid neuropathy: An ALS mimicker
title_full Tongue atrophy and fasciculations in transthyretin familial amyloid neuropathy: An ALS mimicker
title_fullStr Tongue atrophy and fasciculations in transthyretin familial amyloid neuropathy: An ALS mimicker
title_full_unstemmed Tongue atrophy and fasciculations in transthyretin familial amyloid neuropathy: An ALS mimicker
title_short Tongue atrophy and fasciculations in transthyretin familial amyloid neuropathy: An ALS mimicker
title_sort tongue atrophy and fasciculations in transthyretin familial amyloid neuropathy: an als mimicker
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4807904/
https://www.ncbi.nlm.nih.gov/pubmed/27066555
http://dx.doi.org/10.1212/NXG.0000000000000018
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