Eye movement abnormalities in a patient with Zellweger spectrum disorder.

Rosini, F; Vinciguerra, C; Mignarri, A; Di Giovanni, M; Federico, A; Rufa, A

Rosini, F; Vinciguerra, C; Mignarri, A; Di Giovanni, M; Federico, A; Rufa, A.

Afiliación

Rosini F; Eye Tracking and Visual Application Lab (EVALab), Unit of Clinical Neurology and Neurometabolic Diseases, Department of Medicine, Surgery and Neurosciences, University of Siena, Viale Bracci 2, Policlinico Santa Maria alle Scotte, 53100, Siena, Italy.
Vinciguerra C; Unit of Clinical Neurology and Neurometabolic Diseases, Department of Medicine, Surgery and Neurosciences, University of Siena, viale Bracci 2, Policlinico Santa Maria alle Scotte, 53100, Siena, Italy.
Mignarri A; Unit of Clinical Neurology and Neurometabolic Diseases, Department of Medicine, Surgery and Neurosciences, University of Siena, viale Bracci 2, Policlinico Santa Maria alle Scotte, 53100, Siena, Italy.
Di Giovanni M; Unit of Clinical Neurology and Neurometabolic Diseases, Department of Medicine, Surgery and Neurosciences, University of Siena, viale Bracci 2, Policlinico Santa Maria alle Scotte, 53100, Siena, Italy.
Federico A; Unit of Clinical Neurology and Neurometabolic Diseases, Department of Medicine, Surgery and Neurosciences, University of Siena, viale Bracci 2, Policlinico Santa Maria alle Scotte, 53100, Siena, Italy.
Rufa A; Eye Tracking and Visual Application Lab (EVALab), Unit of Clinical Neurology and Neurometabolic Diseases, Department of Medicine, Surgery and Neurosciences, University of Siena, Viale Bracci 2, Policlinico Santa Maria alle Scotte, 53100, Siena, Italy. rufa@unisi.it.

Neurol Sci ; 37(6): 1013-5, 2016 Jun.

Article en En | MEDLINE | ID: mdl-26850714

Asunto(s)

Trastornos de la Motilidad Ocular/complicaciones; Síndrome de Zellweger/complicaciones; Humanos; Masculino; Proteínas de la Membrana/genética; Persona de Mediana Edad; Mutación/genética; Trastornos de la Motilidad Ocular/genética; Factor 2 de la Biogénesis del Peroxisoma; Tiempo de Reacción/fisiología; Síndrome de Zellweger/genética

Palabras clave

Eye movement abnormalities; Gaze-evoked nystagmus; Peroxisomal diseases; Zellweger spectrum disorders

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome de Zellweger / Trastornos de la Motilidad Ocular Límite: Humans / Male / Middle aged Idioma: En Revista: Neurol Sci Asunto de la revista: NEUROLOGIA Año: 2016 Tipo del documento: Article País de afiliación: Italia

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