Hereditary gelsolin amyloidosis (HGA): a neglected cause of bilateral progressive or recurrent facial palsy.

Sagnelli, Anna; Piscosquito, Giuseppe; Di Bella, Daniela; Fadda, Laura; Melzi, Lisa; Morico, Antonio; Ciano, Claudia; Taroni, Franco; Facchetti, Dante; Salsano, Ettore; Pareyson, Davide

Sagnelli, Anna; Piscosquito, Giuseppe; Di Bella, Daniela; Fadda, Laura; Melzi, Lisa; Morico, Antonio; Ciano, Claudia; Taroni, Franco; Facchetti, Dante; Salsano, Ettore; Pareyson, Davide.

Afiliación

Sagnelli A; Department of Clinical Neurosciences, IRCCS Foundation, "C. Besta" Neurological Institute, Milan, Italy.
Piscosquito G; Department of Clinical Neurosciences, IRCCS Foundation, "C. Besta" Neurological Institute, Milan, Italy.
Di Bella D; Department of Diagnostic and Applied Technology, IRCCS Foundation, "C. Besta" Neurological Institute, Milan, Italy.
Fadda L; Department of Neurology, University of Cagliari, Cagliari, Italy.
Melzi L; Department of Ophthalmology, Neuro-ophthalmology Unit, Milan, Italy.
Morico A; Department of Ophthalmology, Corneal Service, IRCCS Istituto Auxologico Italiano, Milan, Italy.
Ciano C; Department of Diagnostic and Applied Technology, IRCCS Foundation, "C. Besta" Neurological Institute, Milan, Italy.
Taroni F; Department of Diagnostic and Applied Technology, IRCCS Foundation, "C. Besta" Neurological Institute, Milan, Italy.
Facchetti D; Department of Neurology, ASST Niguarda Hospital, Milan, Italy.
Salsano E; Department of Clinical Neurosciences, IRCCS Foundation, "C. Besta" Neurological Institute, Milan, Italy.
Pareyson D; Department of Clinical Neurosciences, IRCCS Foundation, "C. Besta" Neurological Institute, Milan, Italy.

J Peripher Nerv Syst ; 22(1): 59-63, 2017 03.

Article en En | MEDLINE | ID: mdl-27982499

Asunto(s)

Amiloidosis Familiar/complicaciones; Amiloidosis Familiar/genética; Parálisis Facial/etiología; Gelsolina/genética; Mutación/genética; Adulto; Progresión de la Enfermedad; Salud de la Familia; Humanos; Masculino

Palabras clave

amyloidosis; bilateral facial palsy; familial amyloid polyneuropathy type IV; hereditary gelsolin amyloidosis; lattice corneal dystrophy

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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Gelsolina / Amiloidosis Familiar / Parálisis Facial / Mutación Límite: Adult / Humans / Male Idioma: En Revista: J Peripher Nerv Syst Asunto de la revista: NEUROLOGIA Año: 2017 Tipo del documento: Article País de afiliación: Italia

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