Literature DB >> 26849231

Epidemiologic Study of Charcot-Marie-Tooth Disease: A Systematic Review.

Lidiane Carine Lima Santos Barreto1, Fernanda Santos Oliveira, Paula Santos Nunes, Iandra Maria Pinheiro de França Costa, Catarina Andrade Garcez, Gabriel Mattos Goes, Eduardo Luis Aquino Neves, Jullyana de Souza Siqueira Quintans, Adriano Antunes de Souza Araújo.   

Abstract

BACKGROUND: Charcot-Marie-Tooth disease (CMT) is the most common inherited neuropathy. CMT is classified into 2 main subgroups: CMT type 1 (CMT1; demyelinating form) and CMT type 2 (CMT2; axonal form). The objectives of this study were to systematically review and assess the quality of studies reporting the incidence and/or prevalence of CMT worldwide.
SUMMARY: A total of 802 studies were initially identified, with only 12 meeting the inclusion criteria. CMT prevalence was reported in 10 studies and ranged from 9.7/100,000 in Serbia to 82.3/100,000 in Norway. The frequency of the main subtypes varied from 37.6 to 84% for CMT1 and from 12 to 35.9% for CMT2; the country with the lowest prevalence of CMT1 was Norway, and the country with the highest prevalence of CMT1 was Iceland; on the other hand, CMT2 was least prevalent in the United Kingdom and most prevalent in Norway. KEY MESSAGES: This review reveals the gaps that still exist in the epidemiological knowledge of CMT around the world. Published studies are of varying quality and utilise different methodologies, thus precluding a robust conclusion. Additional research focusing on epidemiological features of CMT in different nations and different ethnic groups is needed.
© 2016 S. Karger AG, Basel.

Entities:  

Mesh:

Year:  2016        PMID: 26849231     DOI: 10.1159/000443706

Source DB:  PubMed          Journal:  Neuroepidemiology        ISSN: 0251-5350            Impact factor:   3.282


  53 in total

1.  Functional results and quality of life after joint preserving or sacrificing surgery in Charcot-Marie-Tooth foot deformities.

Authors:  Sergio Tejero; Juan Chans-Veres; Andrés Carranza-Bencano; Ahmed E Galhoum; Daniel Poggio; Victor Valderrábano; Mario Herrera-Pérez
Journal:  Int Orthop       Date:  2021-02-21       Impact factor: 3.075

2.  Yield of next-generation neuropathy gene panels in axonal neuropathies.

Authors:  Diana C Lee; Lois Dankwa; Christyn Edmundson; David R Cornblath; Steven S Scherer
Journal:  J Peripher Nerv Syst       Date:  2019-11-19       Impact factor: 3.494

3.  Whole exome sequencing reveals a broader variant spectrum of Charcot-Marie-Tooth disease type 2.

Authors:  Shan Lin; Liu-Qing Xu; Guo-Rong Xu; Ling-Ling Guo; Bi-Juan Lin; Wan-Jin Chen; Ning Wang; Yi Lin; Jin He
Journal:  Neurogenetics       Date:  2019-12-12       Impact factor: 2.660

4.  Charcot-Marie-Tooth disease: genetic subtypes in the Sardinian population.

Authors:  Lorena Lorefice; Maria Rita Murru; Giancarlo Coghe; Giuseppe Fenu; Daniela Corongiu; Jessica Frau; Stefania Tranquilli; Paolo Tacconi; Alessandro Vannelli; Giovanni Marrosu; Elena Mamusa; Eleonora Cocco; Maria Giovanna Marrosu
Journal:  Neurol Sci       Date:  2017-03-13       Impact factor: 3.307

5.  Diffusion tensor imaging of the sciatic nerve in Charcot-Marie-Tooth disease type I patients: a prospective case-control study.

Authors:  Hyun Su Kim; Young Cheol Yoon; Byung-Ok Choi; Wook Jin; Jang Gyu Cha; Jae-Hun Kim
Journal:  Eur Radiol       Date:  2019-01-11       Impact factor: 5.315

6.  [Analysis of GDAP1 gene mutation in a pedigree with autosomal dominant Charcot-Marie-Tooth disease].

Authors:  Li Qin; Canhong Yang; Tianming Lü; Lanying Li; Dandan Zong; Yueying Wu
Journal:  Nan Fang Yi Ke Da Xue Xue Bao       Date:  2019-01-30

7.  PMP22 Gene-Associated Neuropathies: Phenotypic Spectrum in a Cohort from India.

Authors:  Madhu Nagappa; Shivani Sharma; Periyasamy Govindaraj; Yasha T Chickabasaviah; Ramesh Siram; Akhilesh Shroti; Monojit Debnath; Sanjib Sinha; Parayil S Bindu; Arun B Taly
Journal:  J Mol Neurosci       Date:  2020-01-28       Impact factor: 3.444

8.  Mutation update for myelin protein zero-related neuropathies and the increasing role of variants causing a late-onset phenotype.

Authors:  Ilaria Callegari; C Gemelli; A Geroldi; F Veneri; P Mandich; M D'Antonio; D Pareyson; M E Shy; A Schenone; V Prada; M Grandis
Journal:  J Neurol       Date:  2019-07-05       Impact factor: 4.849

9.  Neurological safety of oxaliplatin in patients with uncommon variants in Charcot-Marie-tooth disease genes.

Authors:  Jennifer G Le-Rademacher; Camden L Lopez; Rahul Kanwar; Brittny Major-Elechi; Alexej Abyzov; Michaela S Banck; Terry M Therneau; Jeff A Sloan; Charles L Loprinzi; Andreas S Beutler
Journal:  J Neurol Sci       Date:  2020-01-14       Impact factor: 3.181

10.  Translation and cross-cultural adaptation of the Charcot-Marie-Tooth disease Pediatric Scale to Brazilian Portuguese and determination of its measurement properties.

Authors:  Karoliny Lisandra Teixeira Cruz; Ana Cristina Resende Camargos; Juliana Cardoso; Cyntia Rogean de Jesus Alves de Baptista; Aline Duprat Ramos; Ana Claudia Mattiello-Sverzut; Joshua Burns; Hércules Ribeiro Leite
Journal:  Braz J Phys Ther       Date:  2020-08-07       Impact factor: 3.377

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