Literature DB >> 23963961

Genetic testing practices for Charcot-Marie-Tooth type 1A disease.

Renee Tousignant1, Angela Trepanier, Michael E Shy, Carly E Siskind.   

Abstract

INTRODUCTION: Charcot-Marie-Tooth disease type 1A (CMT1A) is caused by a PMP22 gene duplication. CMT1A has a robust electrical phenotype that can be used to direct genetic testing. We compared specialty CMT center CMT1A diagnosis rates to those of outside physicians.
METHODS: Charts were reviewed for 102 patients with CMT1A seen at a specialty CMT clinic between 2001 and 2009. Nerve conduction studies, family history, date of genetic testing, and type of genetic testing (single gene vs. panel) were collected.
RESULTS: Although the specialty clinic ordered more PMP22 duplication testing alone beginning at an earlier year, thereby reducing costs, both the specialty clinic and outside physicians began the decade doing panel testing and ended the decade looking at only PMP22.
CONCLUSIONS: Specialty centers adapt earlier to changes in testing practice than non-specialty centers. As the landscape of genetic testing changes, the algorithms for testing will also likely change.
Copyright © 2013 Wiley Periodicals, Inc.

Entities:  

Keywords:  CMT1A; Charcot-Marie-Tooth 1A; PMP22 duplication; genetic testing; genetic testing practice

Mesh:

Substances:

Year:  2013        PMID: 23963961     DOI: 10.1002/mus.23991

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


  3 in total

1.  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

2.  Next-generation sequencing and genetic diagnosis of Charcot-Marie-Tooth disease.

Authors:  Ashok Verma
Journal:  Ann Indian Acad Neurol       Date:  2014-10       Impact factor: 1.383

3.  Cell transplantation strategies for acquired and inherited disorders of peripheral myelin.

Authors:  A K M G Muhammad; Kevin Kim; Irina Epifantseva; Arwin Aghamaleky-Sarvestany; Megan E Simpkinson; Sharon Carmona; Jesse Landeros; Shaughn Bell; John Svaren; Robert H Baloh
Journal:  Ann Clin Transl Neurol       Date:  2018-01-22       Impact factor: 4.511

  3 in total

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