Negative myoclonus causes locomotory disability in progressive myoclonus epilepsy type EPM1- Unverricht-Lundborg disease.

Vogt, Heinrich; Baisch, Thomas; Mueller-Pfeiffer, Christoph; Mothersill, Ian William

Vogt, Heinrich; Baisch, Thomas; Mueller-Pfeiffer, Christoph; Mothersill, Ian William.

Afiliação

Vogt H; Swiss Epilepsy Center, Clinic Lengg, Zurich, Switzerland.
Baisch T; Swiss Epilepsy Center, Clinic Lengg, Zurich, Switzerland.
Mueller-Pfeiffer C; Department of Consultation Liaison Psychiatry and Psychosomatic Medicine, University Hospital Zurich, Zurich, Switzerland.
Mothersill IW; Swiss Epilepsy Center, Clinic Lengg, Zurich, Switzerland.

Epileptic Disord ; 25(3): 297-308, 2023 Jun.

Article em En | MEDLINE | ID: mdl-37536959

Assuntos

Mioclonia; Síndrome de Unverricht-Lundborg; Humanos; Síndrome de Unverricht-Lundborg/genética; Mutação; Ataxia; Cistatina B/genética

Palavras-chave

Aetiology: Genetic disorder; EPM1/UnverrichtLundborg disease; Localization: Innervated muscle groups; Phenomenology: Negative myoclonus, teetering/bouncing gait, standing instability; Syndrome: EPM1/Unverricht Lundborg disease; ataxia; locomotory disability (LMD); negative myoclonus (NM); progressive myoclonus epilepsy (PME); silent period (SP)

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Unverricht-Lundborg / Mioclonia Tipo de estudo: Etiology_studies Limite: Humans Idioma: En Revista: Epileptic Disord Assunto da revista: CEREBRO / NEUROLOGIA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Suíça

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