Holmes Tremor‐Like Phenotype in DYT1 Dystonia
Holmes tremor is characterized by a combination of a flexion‐extension resting postural and action tremor, most often due to mesencephalic lesions affecting the nigrostriatal and cerebello‐thalamo‐cortical pathways. On the other hand, dystonic tremor represents a jerky postural and action tremor, wh...
| Autores: | , , , |
|---|---|
| Tipo de documento: | artigo |
| Estado: | Versão publicada |
| Data de publicação: | 2018 |
| País: | Argentina |
| Recursos: | Consejo Nacional de Investigaciones Científicas y Técnicas |
| Repositório: | CONICET Digital (CONICET) |
| Idioma: | inglês |
| OAI Identifier: | oai:ri.conicet.gov.ar:11336/88558 |
| Acesso em linha: | http://hdl.handle.net/11336/88558 |
| Access Level: | Acceso aberto |
| Palavra-chave: | DYSTONIA GENOMICS https://purl.org/becyt/ford/3.2 https://purl.org/becyt/ford/3 |
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Holmes Tremor‐Like Phenotype in DYT1 DystoniaRodríguez Quiroga, Sergio AlejandroGonzález Morón, DoloresEspay, Alberto JKauffman, Marcelo AndresDYSTONIAGENOMICShttps://purl.org/becyt/ford/3.2https://purl.org/becyt/ford/3Holmes tremor is characterized by a combination of a flexion‐extension resting postural and action tremor, most often due to mesencephalic lesions affecting the nigrostriatal and cerebello‐thalamo‐cortical pathways. On the other hand, dystonic tremor represents a jerky postural and action tremor, which if severe enough may include a resting component and may arise from cerebellar and nigrostriatal dysfunction. Here, we present a patient with a four‐decade history of progressive tremor, initially interpreted as Holmes tremor with a dystonic (pseudospastic) gait, in whom whole exome sequencing (WES) demonstrated a pathogenic TOR1A deletion. This case highlights two important clinical points, (1) the need for proper semiologic interpretation: direct DYT1 testing could have been entertained if tremor was properly categorized as dystonic rather than cerebellar at the outset; and (2) the phenotypic variability of DYT1 dystonia, with tremor as a presenting and disabling feature separate from the body part affected by dystonia (“tremor associated with dystonia”).Fil: Rodríguez Quiroga, Sergio Alejandro. Gobierno de la Ciudad de Buenos Aires. Hospital General de Agudos "Ramos Mejía"; ArgentinaFil: González Morón, Dolores. Gobierno de la Ciudad de Buenos Aires. Hospital General de Agudos "Ramos Mejía"; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Espay, Alberto J. University of Cincinnati; Estados UnidosFil: Kauffman, Marcelo Andres. Universidad Austral. Facultad de Ciencias Biomédicas. Instituto de Investigaciones en Medicina Traslacional. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones en Medicina Traslacional; ArgentinaWiley2018-02info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/88558Rodríguez Quiroga, Sergio Alejandro; González Morón, Dolores; Espay, Alberto J; Kauffman, Marcelo Andres; Holmes Tremor‐Like Phenotype in DYT1 Dystonia; Wiley; Movement Disorders Clinical Practice; 5; 2; 2-2018; 206-2082330-1619CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1002/mdc3.12585info:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/full/10.1002/mdc3.12585info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2024-05-08T14:18:06Zoai:ri.conicet.gov.ar:11336/88558instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982024-05-08 14:18:06.474CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
| dc.title.none.fl_str_mv |
Holmes Tremor‐Like Phenotype in DYT1 Dystonia |
| title |
Holmes Tremor‐Like Phenotype in DYT1 Dystonia |
| spellingShingle |
Holmes Tremor‐Like Phenotype in DYT1 Dystonia Rodríguez Quiroga, Sergio Alejandro DYSTONIA GENOMICS https://purl.org/becyt/ford/3.2 https://purl.org/becyt/ford/3 |
| title_short |
Holmes Tremor‐Like Phenotype in DYT1 Dystonia |
| title_full |
Holmes Tremor‐Like Phenotype in DYT1 Dystonia |
| title_fullStr |
Holmes Tremor‐Like Phenotype in DYT1 Dystonia |
| title_full_unstemmed |
Holmes Tremor‐Like Phenotype in DYT1 Dystonia |
| title_sort |
Holmes Tremor‐Like Phenotype in DYT1 Dystonia |
| dc.creator.none.fl_str_mv |
Rodríguez Quiroga, Sergio Alejandro González Morón, Dolores Espay, Alberto J Kauffman, Marcelo Andres |
| author |
Rodríguez Quiroga, Sergio Alejandro |
| author_facet |
Rodríguez Quiroga, Sergio Alejandro González Morón, Dolores Espay, Alberto J Kauffman, Marcelo Andres |
| author_role |
author |
| author2 |
González Morón, Dolores Espay, Alberto J Kauffman, Marcelo Andres |
| author2_role |
author author author |
| dc.subject.none.fl_str_mv |
DYSTONIA GENOMICS https://purl.org/becyt/ford/3.2 https://purl.org/becyt/ford/3 |
| topic |
DYSTONIA GENOMICS https://purl.org/becyt/ford/3.2 https://purl.org/becyt/ford/3 |
| description |
Holmes tremor is characterized by a combination of a flexion‐extension resting postural and action tremor, most often due to mesencephalic lesions affecting the nigrostriatal and cerebello‐thalamo‐cortical pathways. On the other hand, dystonic tremor represents a jerky postural and action tremor, which if severe enough may include a resting component and may arise from cerebellar and nigrostriatal dysfunction. Here, we present a patient with a four‐decade history of progressive tremor, initially interpreted as Holmes tremor with a dystonic (pseudospastic) gait, in whom whole exome sequencing (WES) demonstrated a pathogenic TOR1A deletion. This case highlights two important clinical points, (1) the need for proper semiologic interpretation: direct DYT1 testing could have been entertained if tremor was properly categorized as dystonic rather than cerebellar at the outset; and (2) the phenotypic variability of DYT1 dystonia, with tremor as a presenting and disabling feature separate from the body part affected by dystonia (“tremor associated with dystonia”). |
| publishDate |
2018 |
| dc.date.none.fl_str_mv |
2018-02 |
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info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
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article |
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publishedVersion |
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http://hdl.handle.net/11336/88558 Rodríguez Quiroga, Sergio Alejandro; González Morón, Dolores; Espay, Alberto J; Kauffman, Marcelo Andres; Holmes Tremor‐Like Phenotype in DYT1 Dystonia; Wiley; Movement Disorders Clinical Practice; 5; 2; 2-2018; 206-208 2330-1619 CONICET Digital CONICET |
| url |
http://hdl.handle.net/11336/88558 |
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Rodríguez Quiroga, Sergio Alejandro; González Morón, Dolores; Espay, Alberto J; Kauffman, Marcelo Andres; Holmes Tremor‐Like Phenotype in DYT1 Dystonia; Wiley; Movement Disorders Clinical Practice; 5; 2; 2-2018; 206-208 2330-1619 CONICET Digital CONICET |
| dc.language.none.fl_str_mv |
eng |
| language |
eng |
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info:eu-repo/semantics/altIdentifier/doi/10.1002/mdc3.12585 info:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/full/10.1002/mdc3.12585 |
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info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
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openAccess |
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application/pdf application/pdf |
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Wiley |
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Wiley |
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dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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