Neuro‐Behcet's disease presenting as solitary midbrain lesion with paroxysmal ataxia and dysarthria (PAD) case report

Paroxysmal dysarthria and ataxia (PDA) is a rare neurological manifestation of stereotyped attacks of sudden ataxic symptoms lasts for few seconds to minutes. We report a case of PDA in a 61‐year‐old male with a solitary homogenously enhancing solitary midbrain lesion and positive HLA‐B51 (Allele 2)...

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Autores principales: Sabry Safan, Abeer, EL Beltagi, Ahmed, El Sotouhy, Ahmed, Yagan, Lina, Abunaib, Mohammed, Adeli, Gholam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9020170/
https://www.ncbi.nlm.nih.gov/pubmed/35474991
http://dx.doi.org/10.1002/ccr3.5626
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author Sabry Safan, Abeer
EL Beltagi, Ahmed
El Sotouhy, Ahmed
Yagan, Lina
Abunaib, Mohammed
Adeli, Gholam
author_facet Sabry Safan, Abeer
EL Beltagi, Ahmed
El Sotouhy, Ahmed
Yagan, Lina
Abunaib, Mohammed
Adeli, Gholam
author_sort Sabry Safan, Abeer
collection PubMed
description Paroxysmal dysarthria and ataxia (PDA) is a rare neurological manifestation of stereotyped attacks of sudden ataxic symptoms lasts for few seconds to minutes. We report a case of PDA in a 61‐year‐old male with a solitary homogenously enhancing solitary midbrain lesion and positive HLA‐B51 (Allele 2), controlled with lacosamide.
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spelling pubmed-90201702022-04-25 Neuro‐Behcet's disease presenting as solitary midbrain lesion with paroxysmal ataxia and dysarthria (PAD) case report Sabry Safan, Abeer EL Beltagi, Ahmed El Sotouhy, Ahmed Yagan, Lina Abunaib, Mohammed Adeli, Gholam Clin Case Rep Case Reports Paroxysmal dysarthria and ataxia (PDA) is a rare neurological manifestation of stereotyped attacks of sudden ataxic symptoms lasts for few seconds to minutes. We report a case of PDA in a 61‐year‐old male with a solitary homogenously enhancing solitary midbrain lesion and positive HLA‐B51 (Allele 2), controlled with lacosamide. John Wiley and Sons Inc. 2022-04-20 /pmc/articles/PMC9020170/ /pubmed/35474991 http://dx.doi.org/10.1002/ccr3.5626 Text en © 2022 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. 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
Sabry Safan, Abeer
EL Beltagi, Ahmed
El Sotouhy, Ahmed
Yagan, Lina
Abunaib, Mohammed
Adeli, Gholam
Neuro‐Behcet's disease presenting as solitary midbrain lesion with paroxysmal ataxia and dysarthria (PAD) case report
title Neuro‐Behcet's disease presenting as solitary midbrain lesion with paroxysmal ataxia and dysarthria (PAD) case report
title_full Neuro‐Behcet's disease presenting as solitary midbrain lesion with paroxysmal ataxia and dysarthria (PAD) case report
title_fullStr Neuro‐Behcet's disease presenting as solitary midbrain lesion with paroxysmal ataxia and dysarthria (PAD) case report
title_full_unstemmed Neuro‐Behcet's disease presenting as solitary midbrain lesion with paroxysmal ataxia and dysarthria (PAD) case report
title_short Neuro‐Behcet's disease presenting as solitary midbrain lesion with paroxysmal ataxia and dysarthria (PAD) case report
title_sort neuro‐behcet's disease presenting as solitary midbrain lesion with paroxysmal ataxia and dysarthria (pad) case report
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9020170/
https://www.ncbi.nlm.nih.gov/pubmed/35474991
http://dx.doi.org/10.1002/ccr3.5626
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