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Kearns-Sayre syndrome: expanding spectrum of a "novel" mitochondrial leukomyeloencephalopathy.
Moscatelli, Marco; Ardissone, Anna; Lamantea, Eleonora; Zorzi, Giovanna; Bruno, Claudio; Moroni, Isabella; Erbetta, Alessandra; Chiapparini, Luisa.
Afiliação
  • Moscatelli M; Neuroradiology Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy. marco.moscatelli@istituto-besta.it.
  • Ardissone A; Child Neurology Unit, Department of Pediatric Neuroscience, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
  • Lamantea E; Medical Genetics and Neurogenetics Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
  • Zorzi G; Child Neurology Unit, Department of Pediatric Neuroscience, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
  • Bruno C; Center of Translational and Experimental Myology, IRCCS Istituto Giannina Gaslini, Genova, Italy.
  • Moroni I; Child Neurology Unit, Department of Pediatric Neuroscience, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
  • Erbetta A; Neuroradiology Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
  • Chiapparini L; Neuroradiology Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Neurol Sci ; 43(3): 2081-2084, 2022 Mar.
Article em En | MEDLINE | ID: mdl-35031921
ABSTRACT
Kearns-Sayre syndrome (KSS) is a rare mitochondrial disease associated to a widespread cerebral leukodystrophy. MRI shows a typical centripetal pattern where U-fibers are mainly affected with a relative spare of periventricular white matter. Recently, different patterns of spinal cord involvement have been described in KSS. Here we report 4 new cases with typical cerebral leukodystrophy associated with spinal cord lesions. A pattern characterized by abnormal signal intensity in the H gray matter and posterior columns was found in 2 patients, while the remaining 2 presented a peculiar involvement of the spinal trigeminal nuclei at the junction of low medulla and cervical cord. MRI spinal cord involvement in KSS is probably an underestimated finding and should be evaluated in the diagnostic work up of these patients.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Kearns-Sayre / Doenças Mitocondriais / Substância Branca Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Revista: Neurol Sci Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Kearns-Sayre / Doenças Mitocondriais / Substância Branca Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Revista: Neurol Sci Ano de publicação: 2022 Tipo de documento: Article