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Levodopa-induced belly dancer's dyskinesia: Case report

The first report of an abdominal wall dyskinesia syndrome was published in 1990 by Iliceto et al. (1990), who were the first to use the “belly dancer dyskinesia” (BDD) nomenclature. BDD is a rare syndrome involving repetitive, involuntary, and continuous movements of the abdominal wall muscles (Ilic...

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Autores principales: Cavalcante-Filho, José Renan Miranda, Amâncio-Filho, Walterney, Miniello, Bruno Gonzales
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8298813/
https://www.ncbi.nlm.nih.gov/pubmed/34316648
http://dx.doi.org/10.1016/j.prdoa.2020.100068
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author Cavalcante-Filho, José Renan Miranda
Amâncio-Filho, Walterney
Miniello, Bruno Gonzales
author_facet Cavalcante-Filho, José Renan Miranda
Amâncio-Filho, Walterney
Miniello, Bruno Gonzales
author_sort Cavalcante-Filho, José Renan Miranda
collection PubMed
description The first report of an abdominal wall dyskinesia syndrome was published in 1990 by Iliceto et al. (1990), who were the first to use the “belly dancer dyskinesia” (BDD) nomenclature. BDD is a rare syndrome involving repetitive, involuntary, and continuous movements of the abdominal wall muscles (Iliceto et al., 1990). We describe the case of a 79-year-old, right-handed woman who showed symptoms of BDD syndrome after using levodopa due to parkinson's disease (PD). In this report, BDD was treated by stopping levodopa. After 15 days without levodopa, a positive outcome was achieved. The patient no longer exhibited BDD at the six-month and one-year follow-ups.
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spelling pubmed-82988132021-07-26 Levodopa-induced belly dancer's dyskinesia: Case report Cavalcante-Filho, José Renan Miranda Amâncio-Filho, Walterney Miniello, Bruno Gonzales Clin Park Relat Disord Case Report The first report of an abdominal wall dyskinesia syndrome was published in 1990 by Iliceto et al. (1990), who were the first to use the “belly dancer dyskinesia” (BDD) nomenclature. BDD is a rare syndrome involving repetitive, involuntary, and continuous movements of the abdominal wall muscles (Iliceto et al., 1990). We describe the case of a 79-year-old, right-handed woman who showed symptoms of BDD syndrome after using levodopa due to parkinson's disease (PD). In this report, BDD was treated by stopping levodopa. After 15 days without levodopa, a positive outcome was achieved. The patient no longer exhibited BDD at the six-month and one-year follow-ups. Elsevier 2020-08-14 /pmc/articles/PMC8298813/ /pubmed/34316648 http://dx.doi.org/10.1016/j.prdoa.2020.100068 Text en © 2020 The Authors https://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
Cavalcante-Filho, José Renan Miranda
Amâncio-Filho, Walterney
Miniello, Bruno Gonzales
Levodopa-induced belly dancer's dyskinesia: Case report
title Levodopa-induced belly dancer's dyskinesia: Case report
title_full Levodopa-induced belly dancer's dyskinesia: Case report
title_fullStr Levodopa-induced belly dancer's dyskinesia: Case report
title_full_unstemmed Levodopa-induced belly dancer's dyskinesia: Case report
title_short Levodopa-induced belly dancer's dyskinesia: Case report
title_sort levodopa-induced belly dancer's dyskinesia: case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8298813/
https://www.ncbi.nlm.nih.gov/pubmed/34316648
http://dx.doi.org/10.1016/j.prdoa.2020.100068
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