Literature DB >> 35031921

Kearns-Sayre syndrome: expanding spectrum of a "novel" mitochondrial leukomyeloencephalopathy.

Marco Moscatelli1, Anna Ardissone2, Eleonora Lamantea3, Giovanna Zorzi2, Claudio Bruno4, Isabella Moroni2, Alessandra Erbetta5, Luisa Chiapparini5.   

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.
© 2022. Fondazione Società Italiana di Neurologia.

Entities:  

Keywords:  Kearns-Sayre syndrome; Leukodystrophy; MRI; Mitochondrial disease; Spinal cord

Mesh:

Year:  2022        PMID: 35031921     DOI: 10.1007/s10072-022-05881-8

Source DB:  PubMed          Journal:  Neurol Sci        ISSN: 1590-1874            Impact factor:   3.307


  1 in total

1.  Kearns-Sayre syndrome: a case series of 35 adults and children.

Authors:  Sherezade Khambatta; Douglas L Nguyen; Thomas J Beckman; Christopher M Wittich
Journal:  Int J Gen Med       Date:  2014-07-03
  1 in total

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