Literature DB >> 3195327

Cerebral nuclear magnetic resonance (MRI) in Kearns syndrome.

T Elsås1, P A Rinck, C Isaksen, G Nilsen, O B Schjetne.   

Abstract

We describe an 11-year-old boy with external ophthalmoplegia, pigment retinopathy, hearing loss, elevated spinal protein and ragged-red fibers on muscle biopsy. Cerebral nuclear magnetic resonance (MRI) demonstrated demyelinating lesions in the white matter of the cerebral hemispheres and the cerebellum. To our knowledge this is the first report on the cerebral MRI findings in Kearns syndrome.

Entities:  

Mesh:

Year:  1988        PMID: 3195327     DOI: 10.1111/j.1755-3768.1988.tb04043.x

Source DB:  PubMed          Journal:  Acta Ophthalmol (Copenh)        ISSN: 0001-639X


  3 in total

1.  A case of Kearns-Sayre syndrome with metaphyseal dysplasia.

Authors:  B Wilson; I Claësson; C Forsell; M Tulinius; B Hagberg
Journal:  Pediatr Radiol       Date:  1993

2.  MRI in a case of Kearns-Sayre syndrome confirmed by molecular analysis.

Authors:  G Crisi; G Ferrari; E Merelli; P Cocconcelli
Journal:  Neuroradiology       Date:  1994       Impact factor: 2.804

3.  Early neurological impairment and severe anemia in a newborn with Pearson syndrome.

Authors:  Anne-Sophie Morel; Nadia Joris; Reto Meuli; Sébastien Jacquemont; Diana Ballhausen; Luisa Bonafé; Sarah Fattet; Jean-François Tolsa
Journal:  Eur J Pediatr       Date:  2008-06-14       Impact factor: 3.183

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.