Características clínicas de 63 pacientes con ataxia

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dc.contributor.authorSaffie Awad, Paula
dc.contributor.authorVial Undurraga, Felipe
dc.contributor.authorChaná-Cuevas, Pedro
dc.date.accessioned2022-05-13T20:38:56Z
dc.date.available2022-05-13T20:38:56Z
dc.date.issued2018
dc.description.abstractBackground: Ataxia can be classified as genetic, sporadic or acquired. Aim: To report the clinical features of a group of patients with ataxia. Material and Methods: Review of medical records of patients consulting in a specialized center in movement disorders. Those records in which the diagnosis of “ataxia” or “ataxic syndrome” appeared, were selected for the review. Results: Of 4,282 records surveyed, the diagnosis of ataxia appeared in 95. After eliminating re- peated or incomplete records, 63 were reviewed. Results: Ataxia was sporadic, genetic and acquired in 27, 22 and 14 patients, respectively. The mean age at presentation for genetic, acquired and sporadic ataxia was 24, 46 and 53 years respectively. All autosomal dominant ataxias were type 3 spinocerebellar ataxia (SCA). Friedrich’s ataxia was the most common recessive form. Most sporadic forms of ataxia were multiple system atrophy with predominant cerebellar ataxia (MSA-C) subtype. Conclusions: Considering the heterogeneity of patients with ataxia, we propose a method to approach them.es
dc.description.versionVersión Publicadaes
dc.identifier.citationSaffie Awad P, Vial Undurraga F, Chaná-Cuevas P. Características clínicas de 63 pacientes con ataxia [Clinical features of 63 patients with ataxia]. Rev Med Chil. 2018 Jun;146(6):702-707. Spanish. doi: 10.4067/s0034-98872018000600702. PMID: 30148901.es
dc.identifier.urihttps://doi.org/: 10.4067/s0034-98872018000600702es
dc.identifier.urihttp://hdl.handle.net/11447/6096
dc.language.isoeses
dc.subjectCerebellar Ataxiaes
dc.subjectFriedreich Ataxiaes
dc.subjectMachado-Joseph Diseasees
dc.subjectSpinocerebellar Ataxiases
dc.titleCaracterísticas clínicas de 63 pacientes con ataxiaes
dc.title.alternativeClinical features of 63 patients with ataxiaes
dc.typeArticlees
dcterms.sourceRevista Médica de Chilees

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