Kjellin syndrome: hereditary spastic paraplegia with pathognomonic macular appearance.

Nowak, Victoria Anne; Bremner, Fion; Massey, Luke; Wokke, Beatrijs; Moosavi, Reza; Kara, Eleanna; Houlden, Henry

Nowak, Victoria Anne; Bremner, Fion; Massey, Luke; Wokke, Beatrijs; Moosavi, Reza; Kara, Eleanna; Houlden, Henry.

Afiliação

Nowak VA; Department of Neurosurgery, National Hospital for Neurology and Neurosurgery, London, UK.
Bremner F; Department of Neuro-Ophthalmology, National Hospital for Neurology and Neurosurgery, Queen Square, UK.
Massey L; Department of Neurology, National Hospital for Neurology and Neurosurgery, London, UK.
Wokke B; Department of Neurogenetics, National Hospital for Neurology and Neurosurgery, London, UK.
Moosavi R; Department of Neuro-Ophthalmology, National Hospital for Neurology and Neurosurgery, Queen Square, UK.
Kara E; Reta Lila Weston Laboratories and Department of Molecular Neuroscience, UCL Institute of Neurology, Queen Square, London, UK.
Houlden H; Department of Neurology, National Hospital for Neurology and Neurosurgery, London, UK.

Pract Neurol ; 14(4): 278-9, 2014 Aug.

Article em En | MEDLINE | ID: mdl-24924740

Assuntos

Encéfalo/patologia; Degeneração Retiniana/patologia; Paraplegia Espástica Hereditária/patologia; Adulto; Feminino; Humanos; Degeneração Retiniana/diagnóstico; Paraplegia Espástica Hereditária/diagnóstico

Palavras-chave

Cognition; Heredit Spastic Paraplegia; Neurogenetics; Ophthalmology; Vision

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Degeneração Retiniana / Encéfalo / Paraplegia Espástica Hereditária Tipo de estudo: Diagnostic_studies Limite: Adult / Female / Humans Idioma: En Ano de publicação: 2014 Tipo de documento: Article

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