Literature DB >> 19713553

Quality of life in children with Charcot-Marie-Tooth disease.

Joshua Burns1, Monique M Ryan, Robert A Ouvrier.   

Abstract

The authors studied the health-related quality of life of children aged 5 to 18 years with Charcot-Marie-Tooth disease of varying types and severity and compared it with the general pediatric population. To capture and compare the quality-of-life data across a broad range of ages, the Child Health Questionnaire was completed by parents of 127 children with Charcot-Marie-Tooth disease. Affected children exhibited lower physical, psychological, and social well-being than the general pediatric population, with subsequent worsening of many domains with age. The type of Charcot-Marie-Tooth disease influenced some physical and behavioral quality-of-life domains, while gender, body size, and ethnicity did not. Parent characteristics had generally little impact on the reporting of their child's quality of life, although parents with Charcot-Marie-Tooth disease reported higher bodily pain in their children than those without. Overall, quality of life is negatively affected by the presence and severity of Charcot-Marie-Tooth disease in childhood.

Entities:  

Mesh:

Year:  2009        PMID: 19713553     DOI: 10.1177/0883073809339877

Source DB:  PubMed          Journal:  J Child Neurol        ISSN: 0883-0738            Impact factor:   1.987


  8 in total

1.  The Rare Diseases Clinical Research Network's organization and approach to observational research and health outcomes research.

Authors:  Jeffrey P Krischer; Rashmi Gopal-Srivastava; Stephen C Groft; David J Eckstein
Journal:  J Gen Intern Med       Date:  2014-08       Impact factor: 5.128

2.  Determinants of reduced health-related quality of life in pediatric inherited neuropathies.

Authors:  J Burns; S Ramchandren; M M Ryan; M Shy; R A Ouvrier
Journal:  Neurology       Date:  2010-08-24       Impact factor: 9.910

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

Authors:  Nicholas E Johnson; Janet Sowden; Nuran Dilek; Katy Eichinger; Joshua Burns; Michael P Mcdermott; Michael E Shy; David N Herrmann
Journal:  Muscle Nerve       Date:  2015-02-11       Impact factor: 3.217

4.  Patient identification of the symptomatic impact of charcot-marie-tooth disease type 1A.

Authors:  Nicholas E Johnson; Chad R Heatwole; Michele Ferguson; Janet E Sowden; Shanie Jeanat; David N Herrmann
Journal:  J Clin Neuromuscul Dis       Date:  2013-09

Review 5.  Left to themselves: Time to target chronic pain in childhood rare diseases.

Authors:  Christine B Sieberg; Alyssa Lebel; Erin Silliman; Scott Holmes; David Borsook; Igor Elman
Journal:  Neurosci Biobehav Rev       Date:  2021-03-24       Impact factor: 8.989

6.  Prevalence of Charcot-Marie-Tooth disease across the lifespan: a population-based epidemiological study.

Authors:  Alice Theadom; Richard Roxburgh; Erin MacAulay; Gina O'Grady; Joshua Burns; Priya Parmar; Kelly Jones; Miriam Rodrigues
Journal:  BMJ Open       Date:  2019-06-14       Impact factor: 2.692

7.  Validation of the Italian version of the pediatric CMT quality of life outcome measure.

Authors:  Isabella Moroni; Federica Rachele Danti; Davide Pareyson; Emanuela Pagliano; Giuseppe Piscosquito; Maria Foscan; Alessia Marchi; Anna Ardissone; Silvia Genitrini; Tong Tong Wu; Michael E Shy; Sindhu Ramchandren
Journal:  J Peripher Nerv Syst       Date:  2022-05-03       Impact factor: 5.188

8.  Systematic review of chronic ankle instability in children.

Authors:  Melissa Mandarakas; Fereshteh Pourkazemi; Amy Sman; Joshua Burns; Claire E Hiller
Journal:  J Foot Ankle Res       Date:  2014-03-19       Impact factor: 2.303

  8 in total

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