Literature DB >> 22499103

Novel ANO5 mutations causing hyper-CK-emia, limb girdle muscular weakness and Miyoshi type of muscular dystrophy.

Joachim Schessl1, Wolfram Kress, Benedikt Schoser.   

Abstract

INTRODUCTION: Mutations in the anoctamin 5 gene (ANO5) have been recently identified.They cause limb girdle muscular dystrophy (LGMD2L) and Miyoshi muscular dystrophy.
METHODS: Clinical findings of four unrelated patients are reviewed. Mutation detection was performed by direct sequencing of the ANO5 exons.
RESULTS: We identified four novel mutations in the ANO5 gene. In one patient, a novel homozygous mutation (c.1965G>C). In three patients, the recurrent heterozygous exon 5 c.191dupA mutation is combined with other variants to form a compound heterozygous state: in two cases, novel splice site mutations in intron 5 (c.295-1G>A) and in intron 14 (c.1407+5G>A), and in one case, a novel missense mutation in exon 4 (c.172C>T).
CONCLUSIONS: The cases reported here should help to better understand the important role of mutation screening in the ANO5 gene in patients with adult onset muscular dystrophy and very high CK levels.
Copyright © 2012 Wiley Periodicals, Inc.

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Year:  2012        PMID: 22499103     DOI: 10.1002/mus.23281

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


  14 in total

1.  Sex differences in the involvement of skeletal and cardiac muscles in myopathic Ano5-/- mice.

Authors:  Steven Foltz; Fang Wu; Nasab Ghazal; Jennifer Q Kwong; H Criss Hartzell; Hyojung J Choo
Journal:  Am J Physiol Cell Physiol       Date:  2022-01-12       Impact factor: 4.249

2.  Anoctamin 5 muscular dystrophy in Denmark: prevalence, genotypes, phenotypes, cardiac findings, and muscle protein expression.

Authors:  Nanna Witting; Morten Duno; Helle Petri; Thomas Krag; Henning Bundgaard; Lars Kober; John Vissing
Journal:  J Neurol       Date:  2013-05-14       Impact factor: 4.849

3.  A novel missense mutation in ANO5/TMEM16E is causative for gnathodiaphyseal dyplasia in a large Italian pedigree.

Authors:  Caterina Marconi; Paolo Brunamonti Binello; Giovanni Badiali; Emanuela Caci; Roberto Cusano; Joseph Garibaldi; Tommaso Pippucci; Alberto Merlini; Claudio Marchetti; Kerry J Rhoden; Luis J V Galietta; Faustina Lalatta; Paolo Balbi; Marco Seri
Journal:  Eur J Hum Genet       Date:  2012-10-10       Impact factor: 4.246

4.  Frequency and characterisation of anoctamin 5 mutations in a cohort of Italian limb-girdle muscular dystrophy patients.

Authors:  Francesca Magri; Roberto Del Bo; Maria Grazia D'Angelo; Monica Sciacco; Sandra Gandossini; Alessandra Govoni; Laura Napoli; Patrizia Ciscato; Francesco Fortunato; Erika Brighina; Sara Bonato; Andreina Bordoni; Valeria Lucchini; Stefania Corti; Maurizio Moggio; Nereo Bresolin; Giacomo Pietro Comi
Journal:  Neuromuscul Disord       Date:  2012-06-27       Impact factor: 4.296

5.  Next generation sequencing on patients with LGMD and nonspecific myopathies: Findings associated with ANO5 mutations.

Authors:  Marco Savarese; Giuseppina Di Fruscio; Giorgio Tasca; Lucia Ruggiero; Sandra Janssens; Jan De Bleecker; Marc Delpech; Olimpia Musumeci; Antonio Toscano; Corrado Angelini; Sabrina Sacconi; Lucio Santoro; Enzo Ricci; Kathleen Claes; Luisa Politano; Vincenzo Nigro
Journal:  Neuromuscul Disord       Date:  2015-03-30       Impact factor: 4.296

6.  Genetic disruption of Ano5 in mice does not recapitulate human ANO5-deficient muscular dystrophy.

Authors:  Jing Xu; Mona El Refaey; Li Xu; Lixia Zhao; Yandi Gao; Kyle Floyd; Tallib Karaze; Paul M L Janssen; Renzhi Han
Journal:  Skelet Muscle       Date:  2015-12-21       Impact factor: 4.912

7.  Gnathodiaphyseal dysplasia is not recapitulated in a respective mouse model carrying a mutation of the Ano5 gene.

Authors:  Tim Rolvien; Osman Avci; Simon von Kroge; Till Koehne; Stefan Selbert; Stephan Sonntag; Doron Shmerling; Uwe Kornak; Ralf Oheim; Michael Amling; Thorsten Schinke; Timur Alexander Yorgan
Journal:  Bone Rep       Date:  2020-05-14

8.  First familial limb-girdle muscular dystrophy 2L in China: Clinical, imaging, pathological, and genetic features.

Authors:  Bolin Hu; Li Xiong; Yibiao Zhou; Xiaoqing Lu; Qianqian Xiong; Qing Liu; Xueliang Qi; Weijiang Ding
Journal:  Medicine (Baltimore)       Date:  2018-09       Impact factor: 1.817

9.  Clinical and molecular findings in a cohort of ANO5-related myopathy.

Authors:  André M S Silva; Antônio R Coimbra-Neto; Paulo Victor S Souza; Pablo B Winckler; Marcus V M Gonçalves; Eduardo B U Cavalcanti; Alzira A D S Carvalho; Cláudia F D R Sobreira; Clara G Camelo; Rodrigo D H Mendonça; Eduardo D P Estephan; Umbertina C Reed; Marcela C Machado-Costa; Mario E T Dourado-Junior; Vanessa C Pereira; Marcelo M Cruzeiro; Paulo V P Helito; Laís U Aivazoglou; Leonardo V D Camargo; Hudson H Gomes; Amaro J S D Camargo; Wladimir B V D R Pinto; Bruno M L Badia; Luiz H Libardi; Mario T Yanagiura; Acary S B Oliveira; Anamarli Nucci; Jonas A M Saute; Marcondes C França-Junior; Edmar Zanoteli
Journal:  Ann Clin Transl Neurol       Date:  2019-06-11       Impact factor: 4.511

10.  Whole exome sequencing links dental tumor to an autosomal-dominant mutation in ANO5 gene associated with gnathodiaphyseal dysplasia and muscle dystrophies.

Authors:  T V Andreeva; T V Tyazhelova; V N Rykalina; F E Gusev; A Yu Goltsov; O I Zolotareva; M P Aliseichik; T A Borodina; A P Grigorenko; D A Reshetov; E K Ginter; S S Amelina; R A Zinchenko; E I Rogaev
Journal:  Sci Rep       Date:  2016-05-24       Impact factor: 4.379

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