Literature DB >> 26263471

Update on Charcot-Marie-Tooth disease.

Laurie Gutmann1, Michael Shy.   

Abstract

PURPOSE OF REVIEW: Charcot-Marie-Tooth disease (CMT) is the common terminology used to describe the hereditary neuropathies. This update reviews advances in the past year in our understanding of these diseases, including some important earlier references. RECENT
FINDINGS: In the past year, advances in next-generation sequencing continued to increase the number of genes associated with CMT. The connection between genotype and phenotype has become more complicated. New insights into the pathogenesis of the diseases are reviewed. Treatment and clinical trial updates coming from these new insights, as well as use of high-throughput screening to match potential treatments with targets, are moving the field forward. There is a discussion of potential next steps, including the use of patient-derived induced pluripotent stem cells, to enhance our understanding of individual genotypes and phenotypes.
SUMMARY: The use of high-throughput screens, and techniques such as RNAi and induced pluripotent stem cell continue to push forward other therapies for specific genetic forms of CMT and are potentially more generalizable to peripheral neuropathies. These developments, along with the development of improved outcome measures and longitudinal natural history data, advance CMT, making the future for finding treatments and/or cures closer than it has ever been.

Entities:  

Mesh:

Year:  2015        PMID: 26263471     DOI: 10.1097/WCO.0000000000000237

Source DB:  PubMed          Journal:  Curr Opin Neurol        ISSN: 1350-7540            Impact factor:   5.710


  15 in total

Review 1.  Neurodegenerative Charcot-Marie-Tooth disease as a case study to decipher novel functions of aminoacyl-tRNA synthetases.

Authors:  Na Wei; Qian Zhang; Xiang-Lei Yang
Journal:  J Biol Chem       Date:  2019-01-14       Impact factor: 5.157

2.  Late-Onset Friedreich's Ataxia (LOFA) Mimicking Charcot-Marie-Tooth Disease Type 2: What Is Similar and What Is Different?

Authors:  Rubens Paulo A Salomão; Maria Thereza Drumond Gama; Flávio Moura Rezende Filho; Fernanda Maggi; José Luiz Pedroso; Orlando G P Barsottini
Journal:  Cerebellum       Date:  2017-04       Impact factor: 3.847

3.  CMT disease severity correlates with mutation-induced open conformation of histidyl-tRNA synthetase, not aminoacylation loss, in patient cells.

Authors:  David Blocquel; Litao Sun; Zaneta Matuszek; Sheng Li; Thomas Weber; Bernhard Kuhle; Grace Kooi; Na Wei; Jonathan Baets; Tao Pan; Paul Schimmel; Xiang-Lei Yang
Journal:  Proc Natl Acad Sci U S A       Date:  2019-09-09       Impact factor: 11.205

4.  A multicenter retrospective study of charcot-marie-tooth disease type 4B (CMT4B) associated with mutations in myotubularin-related proteins (MTMRs).

Authors:  Davide Pareyson; Tanya Stojkovic; Mary M Reilly; Sarah Leonard-Louis; Matilde Laurà; Julian Blake; Yesim Parman; Esra Battaloglu; Meriem Tazir; Mounia Bellatache; Nathalie Bonello-Palot; Nicolas Lévy; Sabrina Sacconi; Raquel Guimarães-Costa; Sharham Attarian; Philippe Latour; Guilhem Solé; André Megarbane; Rita Horvath; Giulia Ricci; Byung-Ok Choi; Angelo Schenone; Chiara Gemelli; Alessandro Geroldi; Mario Sabatelli; Marco Luigetti; Lucio Santoro; Fiore Manganelli; Aldo Quattrone; Paola Valentino; Tatsufumi Murakami; Steven S Scherer; Lois Dankwa; Michael E Shy; Chelsea J Bacon; David N Herrmann; Alberto Zambon; Irene Tramacere; Chiara Pisciotta; Stefania Magri; Stefano C Previtali; Alessandra Bolino
Journal:  Ann Neurol       Date:  2019-05-27       Impact factor: 11.274

5.  Clinical and biophysical characterization of 19 GJB1 mutations.

Authors:  Pei-Chien Tsai; De-Ming Yang; Yi-Chu Liao; Tai-Yu Chiu; Hung-Chou Kuo; Yu-Ping Su; Yuh-Cherng Guo; Bing-Wen Soong; Kon-Ping Lin; Yo-Tsen Liu; Yi-Chung Lee
Journal:  Ann Clin Transl Neurol       Date:  2016-09-01       Impact factor: 4.511

6.  Cryptic amyloidogenic elements in mutant NEFH causing Charcot-Marie-Tooth 2 trigger aggresome formation and neuronal death.

Authors:  Arnaud Jacquier; Cécile Delorme; Edwige Belotti; Raoul Juntas-Morales; Guilhem Solé; Odile Dubourg; Marianne Giroux; Claude-Alain Maurage; Valérie Castellani; Adriana Rebelo; Alexander Abrams; Stephan Züchner; Tanya Stojkovic; Laurent Schaeffer; Philippe Latour
Journal:  Acta Neuropathol Commun       Date:  2017-07-14       Impact factor: 7.801

Review 7.  Charcot Marie Tooth 2B Peripheral Sensory Neuropathy: How Rab7 Mutations Impact NGF Signaling?

Authors:  Harry Liu; Chengbiao Wu
Journal:  Int J Mol Sci       Date:  2017-02-04       Impact factor: 5.923

8.  Cell transplantation strategies for acquired and inherited disorders of peripheral myelin.

Authors:  A K M G Muhammad; Kevin Kim; Irina Epifantseva; Arwin Aghamaleky-Sarvestany; Megan E Simpkinson; Sharon Carmona; Jesse Landeros; Shaughn Bell; John Svaren; Robert H Baloh
Journal:  Ann Clin Transl Neurol       Date:  2018-01-22       Impact factor: 4.511

Review 9.  Vocal cord paralysis in Charcot-Marie-Tooth type 4b1 disease associated with a novel mutation in the myotubularin-related protein 2 gene: A case report and review of the literature.

Authors:  Alberto Andrea Zambon; Maria Grazia Natali Sora; Giovanna Cantarella; Federica Cerri; Angelo Quattrini; Giancarlo Comi; Stefano Carlo Previtali; Alessandra Bolino
Journal:  Neuromuscul Disord       Date:  2017-01-16       Impact factor: 4.296

Review 10.  Treating pediatric neuromuscular disorders: The future is now.

Authors:  James J Dowling; Hernan D Gonorazky; Ronald D Cohn; Craig Campbell
Journal:  Am J Med Genet A       Date:  2017-09-10       Impact factor: 2.802

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