Literature DB >> 16051098

Corticospinal tract MRI hyperintensity in X-linked Charcot-Marie-Tooth Disease.

Jan Kassubek1, Volker Bretschneider, Anne-Dorte Sperfeld.   

Abstract

In X-linked hereditary demyelinating neuropathies (CMTX), caused by mutations in Connexin 32, mild subclinical CNS involvement is not unusual. We present a young male patient suffering from genetically proven CMTX who presented with permanent bilateral corticospinal tract hyperintensities in cranial MRI -- a finding previously described to be characteristic for amyotrophic lateral sclerosis. MRI seems to be able to visualize corticospinal tract abnormalities, even if subclinical, in CMTX.

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Year:  2005        PMID： 16051098     DOI： 10.1016/j.jocn.2004.07.020

Source DB:  PubMed          Journal:  J Clin Neurosci        ISSN： 0967-5868            Impact factor:   1.961


  11 in total

Review 1.  The present and the future of neuroimaging in amyotrophic lateral sclerosis.

Authors:  F Agosta; A Chiò; M Cosottini; N De Stefano; A Falini; M Mascalchi; M A Rocca; V Silani; G Tedeschi; M Filippi
Journal:  AJNR Am J Neuroradiol       Date:  2010-04-01       Impact factor: 3.825

Review 2.  Gap junctions in inherited human disorders of the central nervous system.

Authors:  Charles K Abrams; Steven S Scherer
Journal:  Biochim Biophys Acta       Date:  2011-08-16

3.  Motor neuron involvement in anti-Ma2-associated paraneoplastic neurological syndrome.

Authors:  Alberto Vogrig; Bastien Joubert; Aurélien Maureille; Laure Thomas; Emilien Bernard; Nathalie Streichenberger; Francois Cotton; Francois Ducray; Jérome Honnorat
Journal:  J Neurol       Date:  2018-11-29       Impact factor: 4.849

4.  Reversible lesions of the corpus callosum with initially restricted diffusion in a series of Caucasian children.

Authors:  Anthony Le Bras; Maia Proisy; Mathieu Kuchenbuch; Constantin Gomes; Catherine Tréguier; Sylvia Napuri; Emmanuel Quehen; Bertrand Bruneau
Journal:  Pediatr Radiol       Date:  2018-04-17

5.  Human oligodendrocytes express Cx31.3: function and interactions with Cx32 mutants.

Authors:  Irene Sargiannidou; Meejin Ahn; Alan D Enriquez; Alejandro Peinado; Richard Reynolds; Charles Abrams; Steven S Scherer; Kleopas A Kleopa
Journal:  Neurobiol Dis       Date:  2008-02-15       Impact factor: 5.996

6.  CNS involvement in CMTX1 caused by a novel connexin 32 mutation: a 6-year follow-up in neuroimaging and nerve conduction.

Authors:  Chong Xie; Xiajun Zhou; Desheng Zhu; Wei Liu; Xiaoqing Wang; Hong Yang; Zezhi Li; Yong Hao; Guang-Xian Zhang; Yangtai Guan
Journal:  Neurol Sci       Date:  2016-04-20       Impact factor: 3.307

7.  A new mutation in GJC2 associated with subclinical leukodystrophy.

Authors:  Charles K Abrams; Steven S Scherer; Rafael Flores-Obando; Mona M Freidin; Sarah Wong; Eleonora Lamantea; Laura Farina; Vidmer Scaioli; Davide Pareyson; Ettore Salsano
Journal:  J Neurol       Date:  2014-07-25       Impact factor: 4.849

8.  CSF neurofilament light chain reflects corticospinal tract degeneration in ALS.

Authors:  Ricarda A L Menke; Elizabeth Gray; Ching-Hua Lu; Jens Kuhle; Kevin Talbot; Andrea Malaspina; Martin R Turner
Journal:  Ann Clin Transl Neurol       Date:  2015-05-25       Impact factor: 4.511

9.  Voxel-based MRI intensitometry reveals extent of cerebral white matter pathology in amyotrophic lateral sclerosis.

Authors:  Viktor Hartung; Tino Prell; Christian Gaser; Martin R Turner; Florian Tietz; Benjamin Ilse; Martin Bokemeyer; Otto W Witte; Julian Grosskreutz
Journal:  PLoS One       Date:  2014-08-18       Impact factor: 3.240

Review 10.  Connexinopathies: a structural and functional glimpse.

Authors:  Isaac E García; Pavel Prado; Amaury Pupo; Oscar Jara; Diana Rojas-Gómez; Paula Mujica; Carolina Flores-Muñoz; Jorge González-Casanova; Carolina Soto-Riveros; Bernardo I Pinto; Mauricio A Retamal; Carlos González; Agustín D Martínez
Journal:  BMC Cell Biol       Date:  2016-05-24       Impact factor: 4.241
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