Literature DB >> 22810069

Charcot-Marie-Tooth disease and related genetic neuropathies.

Agnes Patzko1, Michael E Shy.   

Abstract

PURPOSE OF REVIEW: The inherited peripheral neuropathies are a complex group of disorders caused by mutations in more than 50 genes. Scientifically, these disorders provide extensive information on molecular pathways that cause demyelination, axonal loss, and abnormal interactions between Schwann cells and the axons they ensheathe. Clinically, however, these neuropathies are confusing because it is difficult to determine what gene to test for in a given patient, inheritance patterns may differ among patients, and genetic testing is expensive. This review provides a biological context and guidelines to help neurologists better understand the basis and focus of genetic testing for these disorders. RECENT
FINDINGS: In the past 5 years, many of the genetic causes of inherited neuropathies have been discovered and the phenotypes of inherited neuropathies have been characterized. Clinical trials of genetic neuropathies are now underway.
SUMMARY: It is hoped that this review will lead to a better understanding of these fascinating neuropathies for health care professionals and that this improved understanding will facilitate treatment advances for these presently untreatable diseases.

Entities:  

Mesh:

Year:  2012        PMID: 22810069     DOI: 10.1212/01.CON.0000411567.34085.da

Source DB:  PubMed          Journal:  Continuum (Minneap Minn)        ISSN: 1080-2371


  10 in total

Review 1.  Peripheral neuropathy: clinical and electrophysiological considerations.

Authors:  Tae Chung; Kalpana Prasad; Thomas E Lloyd
Journal:  Neuroimaging Clin N Am       Date:  2013-05-25       Impact factor: 2.264

2.  Facilitation of Endosomal Recycling by an IRG Protein Homolog Maintains Apical Tubule Structure in Caenorhabditis elegans.

Authors:  Kelly A Grussendorf; Christopher J Trezza; Alexander T Salem; Hikmat Al-Hashimi; Brendan C Mattingly; Drew E Kampmeyer; Liakot A Khan; David H Hall; Verena Göbel; Brian D Ackley; Matthew Buechner
Journal:  Genetics       Date:  2016-06-22       Impact factor: 4.562

3.  CFTR-deficient pigs display peripheral nervous system defects at birth.

Authors:  Leah R Reznikov; Qian Dong; Jeng-Haur Chen; Thomas O Moninger; Jung Min Park; Yuzhou Zhang; Jianyang Du; Michael S Hildebrand; Richard J H Smith; Christoph O Randak; David A Stoltz; Michael J Welsh
Journal:  Proc Natl Acad Sci U S A       Date:  2013-02-04       Impact factor: 11.205

Review 4.  Dysregulation of ErbB Receptor Trafficking and Signaling in Demyelinating Charcot-Marie-Tooth Disease.

Authors:  Samuel M Lee; Lih-Shen Chin; Lian Li
Journal:  Mol Neurobiol       Date:  2016-01-05       Impact factor: 5.590

5.  Exome sequencing reveals HINT1 mutations as a cause of distal hereditary motor neuropathy.

Authors:  Hui Zhao; Valérie Race; Gert Matthijs; Peter De Jonghe; Wim Robberecht; Diether Lambrechts; Philip Van Damme
Journal:  Eur J Hum Genet       Date:  2013-10-09       Impact factor: 4.246

6.  The modified ultrasound pattern sum score mUPSS as additional diagnostic tool for genetically distinct hereditary neuropathies.

Authors:  Alexander Grimm; Maria Rasenack; Ioanna M Athanasopoulou; Nele Maria Dammeier; Christina Lipski; Stefan Wolking; Debora Vittore; Bernhard F Décard; Hubertus Axer
Journal:  J Neurol       Date:  2015-11-11       Impact factor: 4.849

Review 7.  Charcot-Marie-Tooth disease, psychiatric indicators and quality of life: a systematic review.

Authors:  Joana L C Cordeiro; Wilson Marques; Jaime E C Hallak; Flávia L Osório
Journal:  ASN Neuro       Date:  2014-05-27       Impact factor: 4.146

8.  Novel Compound Heterozygous Nonsense PRX Mutations in a Korean Dejerine-Sottas Neuropathy Family.

Authors:  Ye Ji Choi; Young Se Hyun; Soo Hyun Nam; Heasoo Koo; Young Bin Hong; Ki Wha Chung; Byung-Ok Choi
Journal:  J Clin Neurol       Date:  2014-11-11       Impact factor: 3.077

Review 9.  Axonal neuropathy with neuromyotonia: there is a HINT.

Authors:  Kristien Peeters; Teodora Chamova; Ivailo Tournev; Albena Jordanova
Journal:  Brain       Date:  2017-04-01       Impact factor: 13.501

10.  Genotype-phenotype characteristics and baseline natural history of heritable neuropathies caused by mutations in the MPZ gene.

Authors:  Oranee Sanmaneechai; Shawna Feely; Steven S Scherer; David N Herrmann; Joshua Burns; Francesco Muntoni; Jun Li; Carly E Siskind; John W Day; Matilde Laura; Charlotte J Sumner; Thomas E Lloyd; Sindhu Ramchandren; Rosemary R Shy; Tiffany Grider; Chelsea Bacon; Richard S Finkel; Sabrina W Yum; Isabella Moroni; Giuseppe Piscosquito; Davide Pareyson; Mary M Reilly; Michael E Shy
Journal:  Brain       Date:  2015-08-25       Impact factor: 13.501

  10 in total

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