Literature DB >> 28164329

Charcot-Marie-Tooth disease type 1C: Clinical and electrophysiological findings for the c.334G>a (p.Gly112Ser) Litaf/Simple mutation.

Nivedita U Jerath1, Michael E Shy1.   

Abstract

INTRODUCTION: Charcot-Marie-Tooth disease type 1C (CMT1C) is a rare, dominantly inherited neuropathy caused by mutations in the lipopolysaccharide-induced tumor necrosis factor (LITAF) or small integral membrane protein of the lysosome/late endosome (SIMPLE) gene.
METHODS: We present a case series comprised of 10 patients in whom CMT1C is caused by a Gly112Ser substitution in the encoded protein. We focus on clinical presentation, electrodiagnostic analyses, and our findings in the context of previously described cases.
RESULTS: The Gly112Ser mutation causing CMT1C is a mild form of CMT, as patients walked on time, had less weakness than those with Charcot-Marie-Tooth disease type 1A (CMT1A), had a CMT neuropathy score (CMTNS) indicative of mild disease, and had faster ulnar and median motor nerve conduction velocities compared to those with CMT1A. DISCUSSION: The G112S mutation in LITAF seems to be clinically indistinguishable from a mild presentation of CMT1A. Muscle Nerve 56: 1092-1095, 2017.
© 2017 Wiley Periodicals, Inc.

Entities:  

Keywords:  CMT1C; EDx; HMSN type 1; LITAF; SIMPLE; nerve conduction studies

Mesh:

Substances:

Year:  2017        PMID: 28164329      PMCID: PMC5587391          DOI: 10.1002/mus.25600

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  17 in total

1.  European Federation of Neurological Societies/Peripheral Nerve Society Guideline on management of chronic inflammatory demyelinating polyradiculoneuropathy: report of a joint task force of the European Federation of Neurological Societies and the Peripheral Nerve Society--First Revision.

Authors: 
Journal:  J Peripher Nerv Syst       Date:  2010-03       Impact factor: 3.494

2.  Mutations associated with Charcot-Marie-Tooth disease cause SIMPLE protein mislocalization and degradation by the proteasome and aggresome-autophagy pathways.

Authors:  Samuel M Lee; James A Olzmann; Lih-Shen Chin; Lian Li
Journal:  J Cell Sci       Date:  2011-09-06       Impact factor: 5.285

3.  Pain assessment in Charcot-Marie-Tooth (CMT) disease.

Authors:  C Ribiere; M Bernardin; S Sacconi; E Delmont; M Fournier-Mehouas; H Rauscent; M Benchortane; P Staccini; M Lantéri-Minet; C Desnuelle
Journal:  Ann Phys Rehabil Med       Date:  2012-03-06

4.  SIMPLE mutation analysis in dominant demyelinating Charcot-Marie-Tooth disease: three novel mutations.

Authors:  Philippe Latour; Pierre-Marie Gonnaud; Elisabeth Ollagnon; Victor Chan; Serge Perelman; Tanya Stojkovic; Claude Stoll; Christophe Vial; François Ziegler; Antoon Vandenberghe; Irène Maire
Journal:  J Peripher Nerv Syst       Date:  2006-06       Impact factor: 3.494

5.  SIMPLE mutation in demyelinating neuropathy and distribution in sciatic nerve.

Authors:  Craig L Bennett; Andrew J Shirk; Huy M Huynh; Valerie A Street; Eva Nelis; Lionel Van Maldergem; Peter De Jonghe; Albena Jordanova; Velina Guergueltcheva; Ivailo Tournev; Peter Van Den Bergh; Pavel Seeman; Radim Mazanec; Tomas Prochazka; Ivo Kremensky; Jana Haberlova; Michael D Weiss; Vincent Timmerman; Thomas D Bird; Phillip F Chance
Journal:  Ann Neurol       Date:  2004-05       Impact factor: 10.422

6.  Neuropathy progression in Charcot-Marie-Tooth disease type 1A.

Authors:  M E Shy; L Chen; E R Swan; R Taube; K M Krajewski; D Herrmann; R A Lewis; M P McDermott
Journal:  Neurology       Date:  2008-01-29       Impact factor: 9.910

7.  A novel LITAF/SIMPLE mutation within a family with a demyelinating form of Charcot-Marie-Tooth disease.

Authors:  Paola Ciotti; Marco Luigetti; Alessandro Geroldi; Simona Capponi; Ilaria Pezzini; Rossella Gulli; Costanza Pazzaglia; Luca Padua; Roberto Massa; Paola Mandich; Emilia Bellone
Journal:  J Neurol Sci       Date:  2014-05-22       Impact factor: 3.181

8.  Hereditary motor and sensory neuropathy caused by a novel mutation in LITAF.

Authors:  Wanda Maria Gerding; Judith Koetting; Jörg Thomas Epplen; Clemens Neusch
Journal:  Neuromuscul Disord       Date:  2009-06-21       Impact factor: 4.296

9.  CMT subtypes and disease burden in patients enrolled in the Inherited Neuropathies Consortium natural history study: a cross-sectional analysis.

Authors:  V Fridman; B Bundy; M M Reilly; D Pareyson; C Bacon; J Burns; J Day; S Feely; R S Finkel; T Grider; C A Kirk; D N Herrmann; M Laurá; J Li; T Lloyd; C J Sumner; F Muntoni; G Piscosquito; S Ramchandren; R Shy; C E Siskind; S W Yum; I Moroni; E Pagliano; S Zuchner; S S Scherer; M E Shy
Journal:  J Neurol Neurosurg Psychiatry       Date:  2014-11-27       Impact factor: 10.154

10.  LITAF mutations associated with Charcot-Marie-Tooth disease 1C show mislocalization from the late endosome/lysosome to the mitochondria.

Authors:  Andressa Ferreira Lacerda; Emily Hartjes; Craig R Brunetti
Journal:  PLoS One       Date:  2014-07-24       Impact factor: 3.240

View more
  2 in total

Review 1.  New evidence for secondary axonal degeneration in demyelinating neuropathies.

Authors:  Kathryn R Moss; Taylor S Bopp; Anna E Johnson; Ahmet Höke
Journal:  Neurosci Lett       Date:  2020-12-24       Impact factor: 3.046

2.  Rare among Rare: Phenotypes of Uncommon CMT Genotypes.

Authors:  Luca Gentile; Massimo Russo; Federica Taioli; Moreno Ferrarini; M'Hammed Aguennouz; Carmelo Rodolico; Antonio Toscano; Gian Maria Fabrizi; Anna Mazzeo
Journal:  Brain Sci       Date:  2021-12-08
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.