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Neurocognitive profile of patients with X-linked dystonia-parkinsonism.
Jamora, Roland Dominic G; Suratos, Cezar Thomas R; Bautista, Jesi Ellen C; Ramiro, Gail Melissa I; Westenberger, Ana; Klein, Christine; Ledesma, Lourdes K.
Afiliação
  • Jamora RDG; Division of Adult Neurology, Department of Neurosciences, College of Medicine-Philippine General Hospital, University of the Philippines Manila, Taft Ave., Ermita, 1000, Manila, Philippines. rgjamora@up.edu.ph.
  • Suratos CTR; Movement Disorders Service and Section of Neurology, Institute for Neurosciences, St. Luke's Medical Center, Global City, Philippines. rgjamora@up.edu.ph.
  • Bautista JEC; Division of Adult Neurology, Department of Neurosciences, College of Medicine-Philippine General Hospital, University of the Philippines Manila, Taft Ave., Ermita, 1000, Manila, Philippines.
  • Ramiro GMI; Division of Adult Neurology, Department of Neurosciences, College of Medicine-Philippine General Hospital, University of the Philippines Manila, Taft Ave., Ermita, 1000, Manila, Philippines.
  • Westenberger A; Division of Adult Neurology, Department of Neurosciences, College of Medicine-Philippine General Hospital, University of the Philippines Manila, Taft Ave., Ermita, 1000, Manila, Philippines.
  • Klein C; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.
  • Ledesma LK; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.
J Neural Transm (Vienna) ; 128(5): 671-678, 2021 May.
Article em En | MEDLINE | ID: mdl-33638704
ABSTRACT
X-linked dystonia-parkinsonism (XDP) is a debilitating movement disorder endemic to the Panay Island, Philippines. Most studies focus on motor symptoms, hence we reviewed the neurocognitive profile of XDP patients. Neurocognitive testing of XDP patients focused on five domains general intellectual functioning, episodic memory, language, attention and executive function, and affect. Twenty-nine genetically confirmed patients were included. Twenty-six (89.6%) had impairments in one or more domains, while only three had no impairment in any domain. Attention and executive function was the most commonly affected domain (n = 23, 79.3%). Deficits in general intellect, episodic memory, attention and executive function and affect were seen in our subset of XDP patients. The striatal pathology affecting the frontostriatal circuitry mandating these cognitive processes is mainly implicated in these impairments. The results of our study provided further evidence on the extent of cognitive impairment in XDP using a select battery of neurocognitive tests.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Distúrbios Distônicos / Doenças Genéticas Ligadas ao Cromossomo X Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Distúrbios Distônicos / Doenças Genéticas Ligadas ao Cromossomo X Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article