Literature DB >> 25042364

Prospective study of muscle cramps in Charcot-Marie-tooth disease.

Nicholas E Johnson1, Janet Sowden, Nuran Dilek, Katy Eichinger, Joshua Burns, Michael P Mcdermott, Michael E Shy, David N Herrmann.   

Abstract

INTRODUCTION: This study aims to assess the frequency, location, severity, duration, and fluctuation over time of muscle cramps in Charcot-Marie-Tooth disease (CMT).
METHODS: Inherited Neuropathies Consortium Contact Registry participants recorded the occurrence and characteristics of muscle cramps using an 11-question survey administered 3 times over 8 weeks.
RESULTS: A total of 110 adult patients with CMT completed the survey. Weekly cramp frequency was 9.3 (SD 12.3), and 23% had daily muscle cramps. Twenty-two percent reported a significant impact on quality of life. Over 8 weeks, the daily frequency and severity of muscle cramps did not change significantly.
CONCLUSIONS: Patients with CMT have muscle cramps that vary little over an 8-week period, and they may interfere with quality of life. These data may be useful in the planning of clinical trials of agents to treat adults with CMT-associated muscle cramps.
© 2014 Wiley Periodicals, Inc.

Entities:  

Keywords:  CMT symptoms; Charcot-Marie-Tooth disease; RDCRN; Rare Disease Clinical Research Network; longitudinal survey; muscle cramps; quality of life

Mesh:

Year:  2015        PMID: 25042364      PMCID: PMC4860275          DOI: 10.1002/mus.24333

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


  9 in total

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Authors:  J Burns; S Ramchandren; M M Ryan; M Shy; R A Ouvrier
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2.  Muscle cramp in pediatric Charcot-Marie-Tooth disease type 1A: prevalence and predictors.

Authors:  Fiona Blyton; Monique M Ryan; Robert A Ouvrier; Joshua Burns
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3.  Factors associated with night-time calf muscle cramps: a case-control study.

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Review 4.  Muscle cramps.

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Authors:  Fiona Blyton; Vivienne Chuter; Kate E L Walter; Joshua Burns
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7.  Factors that influence health-related quality of life in Australian adults with Charcot-Marie-Tooth disease.

Authors:  Anthony C Redmond; Joshua Burns; Robert A Ouvrier
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Review 8.  Diagnosis and new treatments in genetic neuropathies.

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9.  Estimation of the frequency of the muscular pain-fasciculation syndrome and the muscular cramp-fasciculation syndrome in the adult population.

Authors:  P H Jansen; J A van Dijck; A L Verbeek; F W Durian; E M Joosten
Journal:  Eur Arch Psychiatry Clin Neurosci       Date:  1991       Impact factor: 5.270

  9 in total
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Review 2.  Neurogenic muscle cramps.

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7.  Phenotype of Patients With Charcot-Marie-Tooth With the p.His123Arg Mutation in GDAP1 in Northern Finland.

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8.  Patient-Reported Symptom Burden of Charcot-Marie-Tooth Disease Type 1A: Findings From an Observational Digital Lifestyle Study.

Authors:  Florian P Thomas; Mario A Saporta; Shahram Attarian; Teresa Sevilla; Rafael Sivera; Gian M Fabrizi; Filippo Genovese; Amy J Gray; Simon Bull; Daniel Tanesse; Manuel Rego; Allison Moore; Courtney Hollett; Xavier Paoli; Thomas Sénéchal; Laura Day; Chengyu Ouyang; Samuel Llewellyn; Mark Larkin; Youcef Boutalbi
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9.  Satisfaction with ankle foot orthoses in individuals with Charcot-Marie-Tooth disease.

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Review 10.  The genetics of Charcot-Marie-Tooth disease: current trends and future implications for diagnosis and management.

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