Literature DB >> 23931782

DNA testing in hereditary neuropathies.

Sinéad M Murphy1, Matilde Laurá, Mary M Reilly.   

Abstract

The inherited neuropathies are a clinically and genetically heterogeneous group of disorders in which there have been rapid advances in the last two decades. Molecular genetic testing is now an integral part of the evaluation of patients with inherited neuropathies. In this chapter we describe the genes responsible for the primary inherited neuropathies. We briefly discuss the clinical phenotype of each of the known inherited neuropathy subgroups, describe algorithms for molecular genetic testing of affected patients and discuss genetic counseling. The basic principles of careful phenotyping, documenting an accurate family history, and testing the available genes in an appropriate manner should identify the vast majority of individuals with CMT1 and many of those with CMT2. In this chapter we also describe the current methods of genetic testing. As advances are made in molecular genetic technologies and improvements are made in bioinformatics, it is likely that the current time-consuming methods of DNA sequencing will give way to quicker and more efficient high-throughput methods, which are briefly discussed here.
Copyright © 2013 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Charcot−Marie−Tooth disease (CMT); DNA; genetic counseling; genetic testing; hereditary motor and sensory neuropathy (HMSN); hereditary motor neuropathy (HMN); hereditary sensory and autonomic neuropathy (HSAN); multiplex ligation-dependent probe amplification (MLPA); polymerase chain reaction (PCR)

Mesh:

Year:  2013        PMID: 23931782     DOI: 10.1016/B978-0-444-52902-2.00012-6

Source DB:  PubMed          Journal:  Handb Clin Neurol        ISSN: 0072-9752


  4 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.  Mutations in the Heme Exporter FLVCR1 Cause Sensory Neurodegeneration with Loss of Pain Perception.

Authors:  Deborah Chiabrando; Marco Castori; Maja di Rocco; Martin Ungelenk; Sebastian Gießelmann; Matteo Di Capua; Annalisa Madeo; Paola Grammatico; Sophie Bartsch; Christian A Hübner; Fiorella Altruda; Lorenzo Silengo; Emanuela Tolosano; Ingo Kurth
Journal:  PLoS Genet       Date:  2016-12-06       Impact factor: 5.917

3.  Identification of Genetic Causes of Inherited Peripheral Neuropathies by Targeted Gene Panel Sequencing.

Authors:  Soo Hyun Nam; Young Bin Hong; Young Se Hyun; Da Eun Nam; Geon Kwak; Sun Hee Hwang; Byung-Ok Choi; Ki Wha Chung
Journal:  Mol Cells       Date:  2016-03-30       Impact factor: 5.034

4.  Improving diagnosis of inherited peripheral neuropathies through gene panel analysis.

Authors:  Petra Laššuthová; Dana Šafka Brožková; Marcela Krůtová; Jana Neupauerová; Jana Haberlová; Radim Mazanec; Pavel Dřímal; Pavel Seeman
Journal:  Orphanet J Rare Dis       Date:  2016-08-22       Impact factor: 4.123

  4 in total

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