Literature DB >> 25987458

A comprehensive genetic diagnosis of Chinese muscular dystrophy and congenital myopathy patients by targeted next-generation sequencing.

Yi Dai1, Xiaoming Wei2, Yanhuan Zhao1, Haitao Ren1, Zhangzhang Lan3, Yun Yang2, Lin Chen1, Liying Cui4.   

Abstract

Muscular dystrophies and congenital myopathies are a large group of heterogeneous inherited muscle disorders. The spectrum of muscular dystrophies and congenital myopathies extends to more than 50 diseases today, even excluding the common forms Duchenne Muscular Dystrophy, Myotonic Dystrophy and Facioscapulohumeral Dystrophy. Unfortunately, even by critical clinical evaluation and muscle pathology, diagnosis is still difficult. To potentially remediate this difficulty, we applied a microarray-based targeted next-generation sequencing (NGS) technology to diagnose these patients. There were 55 consecutive unrelated patients who underwent the test, 36 of which (65%) were found to have a causative mutation. Our result shows the accuracy and efficiency of next-generation sequencing in clinical circumstances and reflects the features and relative distribution of inherited myopathies in the Chinese population.
Copyright © 2015 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Chinese patients' features; Congenital myopathy; Muscular dystrophy; Prospective diagnostic study; Targeted next-generation sequencing

Mesh:

Year:  2015        PMID: 25987458     DOI: 10.1016/j.nmd.2015.03.002

Source DB:  PubMed          Journal:  Neuromuscul Disord        ISSN: 0960-8966            Impact factor:   4.296


  18 in total

1.  Utility of a next-generation sequencing-based gene panel investigation in German patients with genetically unclassified limb-girdle muscular dystrophy.

Authors:  Marius Kuhn; Dieter Gläser; Pushpa Raj Joshi; Stephan Zierz; Stephan Wenninger; Benedikt Schoser; Marcus Deschauer
Journal:  J Neurol       Date:  2016-02-17       Impact factor: 4.849

Review 2.  Increasing Role of Titin Mutations in Neuromuscular Disorders.

Authors:  Marco Savarese; Jaakko Sarparanta; Anna Vihola; Bjarne Udd; Peter Hackman
Journal:  J Neuromuscul Dis       Date:  2016-08-30

3.  Exome sequences versus sequential gene testing in the UK highly specialised Service for Limb Girdle Muscular Dystrophy.

Authors:  Elizabeth Harris; Ana Topf; Rita Barresi; Judith Hudson; Helen Powell; James Tellez; Debbie Hicks; Anna Porter; Marta Bertoli; Teresinha Evangelista; Chiara Marini-Betollo; Ólafur Magnússon; Monkol Lek; Daniel MacArthur; Kate Bushby; Hanns Lochmüller; Volker Straub
Journal:  Orphanet J Rare Dis       Date:  2017-09-06       Impact factor: 4.123

4.  Correlation of phenotype with genotype and protein structure in RYR1-related disorders.

Authors:  Joshua J Todd; Vatsala Sagar; Tokunbor A Lawal; Carolyn Allen; Muslima S Razaqyar; Monique S Shelton; Irene C Chrismer; Xuemin Zhang; Mary M Cosgrove; Anna Kuo; Ruhi Vasavada; Minal S Jain; Melissa Waite; Dinusha Rajapakse; Jessica W Witherspoon; Graeme Wistow; Katherine G Meilleur
Journal:  J Neurol       Date:  2018-08-28       Impact factor: 4.849

5.  Diagnosis of late-onset Pompe disease and other muscle disorders by next-generation sequencing.

Authors:  Sébastien Lévesque; Christiane Auray-Blais; Elaine Gravel; Michel Boutin; Laura Dempsey-Nunez; Pierre-Etienne Jacques; Sébastien Chenier; Sandrine Larue; Marie-France Rioux; Walla Al-Hertani; Amelie Nadeau; Jean Mathieu; Bruno Maranda; Valérie Désilets; Paula J Waters; Joan Keutzer; Stephanie Austin; Priya Kishnani
Journal:  Orphanet J Rare Dis       Date:  2016-01-25       Impact factor: 4.123

6.  Improving molecular diagnosis of Chinese patients with Charcot-Marie-Tooth by targeted next-generation sequencing and functional analysis.

Authors:  Li-Xi Li; Shao-Yun Zhao; Zhi-Jun Liu; Wang Ni; Hong-Fu Li; Bao-Guo Xiao; Zhi-Ying Wu
Journal:  Oncotarget       Date:  2016-05-10

7.  A first-line diagnostic assay for limb-girdle muscular dystrophy and other myopathies.

Authors:  Dorota Monies; Hindi N Alhindi; Mohamed A Almuhaizea; Mohamed Abouelhoda; Anas M Alazami; Ewa Goljan; Banan Alyounes; Dyala Jaroudi; Abdulelah AlIssa; Khalid Alabdulrahman; Shazia Subhani; Mohamed El-Kalioby; Tariq Faquih; Salma M Wakil; Nada A Altassan; Brian F Meyer; Saeed Bohlega
Journal:  Hum Genomics       Date:  2016-09-27       Impact factor: 4.639

8.  Diagnostic utility of exome sequencing in the evaluation of neuromuscular disorders.

Authors:  Gloria T Haskell; Michael C Adams; Zheng Fan; Krunal Amin; Roberto J Guzman Badillo; Linran Zhou; Christopher Bizon; Nizar Chahin; Robert S Greenwood; Laura V Milko; Yael Shiloh-Malawsky; Kristy R Crooks; Natasha Strande; Michael Tennison; Christian R Tilley; Alicia Brandt; Kirk C Wilhelmsen; Karen Weck; James P Evans; Jonathan S Berg
Journal:  Neurol Genet       Date:  2018-02-01

9.  Early-Onset LMNA-Associated Muscular Dystrophy with Later Involvement of Contracture.

Authors:  Younggun Lee; Jung Hwan Lee; Hyung Jun Park; Young Chul Choi
Journal:  J Clin Neurol       Date:  2017-10       Impact factor: 3.077

10.  A mutation update for the FLNC gene in myopathies and cardiomyopathies.

Authors:  Job A J Verdonschot; Els K Vanhoutte; Godelieve R F Claes; Apollonia T J M Helderman-van den Enden; Janneke G J Hoeijmakers; Debby M E I Hellebrekers; Amber de Haan; Imke Christiaans; Ronald H Lekanne Deprez; Hanne M Boen; Emeline M van Craenenbroeck; Bart L Loeys; Yvonne M Hoedemaekers; Carlo Marcelis; Marlies Kempers; Esther Brusse; Jaap I van Waning; Annette F Baas; Dennis Dooijes; Folkert W Asselbergs; Daniela Q C M Barge-Schaapveld; Pieter Koopman; Arthur van den Wijngaard; Stephane R B Heymans; Ingrid P C Krapels; Han G Brunner
Journal:  Hum Mutat       Date:  2020-03-20       Impact factor: 4.878

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