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dc.contributor.authorBocanegra García, Orfa Yamile-
dc.contributor.authorBáez Buitrago, Sandra Jimena-
dc.contributor.authorCouto, Blas-
dc.contributor.authorHerrera Murcia, Eduar-
dc.contributor.authorTrujillo Orrego, Natalia-
dc.contributor.authorMadrigal Zapata, Lucia del Socorro-
dc.contributor.authorCardona Londoño, Juan Felipe-
dc.contributor.authorManes, Facundo-
dc.contributor.authorIbañez Barassi, Agustín-
dc.contributor.authorVillegas Lanau, Carlos Andrés-
dc.date.accessioned2023-02-16T21:15:53Z-
dc.date.available2023-02-16T21:15:53Z-
dc.date.issued2013-
dc.identifier.issn1663-4365-
dc.identifier.urihttps://hdl.handle.net/10495/33512-
dc.description.abstractABSTRACT: Cockayne syndrome (CS) is an autosomal recessive disease associated with premature aging, progressive multiorgan degeneration, and nervous system abnormalities including cerebral and cerebellar atrophy, brain calcifications, and white matter abnormalities. Although several clinical descriptions of CS patients have reported developmental delay and cognitive impairment with relative preservation of social skills, no previous studies have carried out a comprehensive neuropsychological and social cognition assessment. Furthermore, no previous research in individuals with CS has examined the relationship between brain atrophy and performance on neuropsychological and social cognition tests. This study describes the case of an atypical late-onset type III CS patient who exceeds the mean life expectancy of individuals with this pathology. The patient and a group of healthy controls underwent a comprehensive assessment that included multiple neuropsychological and social cognition (emotion recognition, theory of mind, and empathy) tasks. In addition, we compared the pattern of atrophy in the patient to controls and to its concordance with ERCC8 gene expression in a healthy brain. The results showed memory, language, and executive deficits that contrast with the relative preservation of social cognition skills. The cognitive profile of the patient was consistent with his pattern of global cerebral and cerebellar loss of gray matter volume (frontal structures, bilateral cerebellum, basal ganglia, temporal lobe, and occipito-temporal/occipito-parietal regions), which in turn was anatomically consistent with the ERCC8 gene expression level in a healthy donor’s brain. The study of exceptional cases, such as the one described here, is fundamental to elucidating the processes that affect the brain in premature aging diseases, and such studies provide an important source of information for understanding the problems associated with normal and pathological aging.spa
dc.format.extent18spa
dc.format.mimetypeapplication/pdfspa
dc.language.isoengspa
dc.publisherFrontiers Mediaspa
dc.type.hasversioninfo:eu-repo/semantics/publishedVersionspa
dc.rightsinfo:eu-repo/semantics/openAccessspa
dc.rights.urihttp://creativecommons.org/licenses/by/2.5/co/*
dc.titleTracking the Cognitive, Social, and Neuroanatomical Profile in Early Neurodegeneration: Type III Cockayne Syndromespa
dc.typeinfo:eu-repo/semantics/articlespa
dc.publisher.groupGrupo Neuropsicología y Conductaspa
dc.publisher.groupGrupo de Neurociencias de Antioquiaspa
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a86spa
dc.rights.accessrightshttp://purl.org/coar/access_right/c_abf2spa
oaire.citationtitleFrontiers in Aging Neurosciencespa
oaire.citationstartpage1spa
oaire.citationendpage18spa
oaire.citationvolume5spa
dc.rights.creativecommonshttps://creativecommons.org/licenses/by/4.0/spa
dc.publisher.placeLausana, Suizaspa
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1spa
dc.type.redcolhttps://purl.org/redcol/resource_type/ARTspa
dc.type.localArtículo de investigaciónspa
dc.subject.decsCockayne Syndrome-
dc.subject.decsSíndrome de Cockayne-
dc.subject.decsCognition-
dc.subject.decsCognición-
dc.subject.decsExecutive Function-
dc.subject.decsFunción Ejecutiva-
dc.description.researchgroupidCOL0007551spa
dc.description.researchgroupidCOL0010744spa
dc.relation.ispartofjournalabbrevFront. Aging. Neurosci.spa
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