Literature DB >> 25182749

Atypical presentation of GNE myopathy with asymmetric hand weakness.

John Karl L de Dios1, Joseph A Shrader2, Galen O Joe2, Jeffrey C McClean3, Kayla Williams2, Robert Evers4, May Christine V Malicdan1, Carla Ciccone1, Ami Mankodi5, Marjan Huizing1, John C McKew6, David A Bluemke4, William A Gahl1, Nuria Carrillo-Carrasco7.   

Abstract

GNE myopathy is a rare autosomal recessive muscle disease caused by mutations in GNE, the gene encoding the rate-limiting enzyme in sialic acid biosynthesis. GNE myopathy usually manifests in early adulthood with distal myopathy that progresses slowly and symmetrically, first involving distal muscles of the lower extremities, followed by proximal muscles with relative sparing of the quadriceps. Upper extremities are typically affected later in the disease. We report a patient with GNE myopathy who presented with asymmetric hand weakness. He had considerably decreased left grip strength, atrophy of the left anterior forearm and fibro-fatty tissue replacement of left forearm flexor muscles on T1-weighted magnetic resonance imaging. The patient was an endoscopist and thus the asymmetric hand involvement may be associated with left hand overuse in daily repetitive pinching and gripping movements, highlighting the possible impact of environmental factors on the progression of genetic muscle conditions. Published by Elsevier B.V.

Entities:  

Keywords:  Distal myopathy with rimmed vacuoles (DMRV); GNE myopathy; Hereditary inclusion body myopathy (HIBM); Inclusion body myopathy 2; N-acetylmannosamine (ManNAc); Nonaka myopathy; Sialic acid

Mesh:

Substances:

Year:  2014        PMID: 25182749      PMCID: PMC4259851          DOI: 10.1016/j.nmd.2014.07.006

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


  23 in total

1.  GNE myopathy: new name and new mutation nomenclature.

Authors:  Marjan Huizing; Nuria Carrillo-Carrasco; May Christine V Malicdan; Satoru Noguchi; William A Gahl; Stella Mitrani-Rosenbaum; Zohar Argov; Ichizo Nishino
Journal:  Neuromuscul Disord       Date:  2014-03-13       Impact factor: 4.296

Review 2.  Mutation update for GNE gene variants associated with GNE myopathy.

Authors:  Frank V Celeste; Thierry Vilboux; Carla Ciccone; John Karl de Dios; May Christine V Malicdan; Petcharat Leoyklang; John C McKew; William A Gahl; Nuria Carrillo-Carrasco; Marjan Huizing
Journal:  Hum Mutat       Date:  2014-08       Impact factor: 4.878

3.  Muscle imaging findings in GNE myopathy.

Authors:  Giorgio Tasca; Enzo Ricci; Mauro Monforte; Francesco Laschena; Pierfrancesco Ottaviani; Carmelo Rodolico; Emanuele Barca; Gabriella Silvestri; Elisabetta Iannaccone; Massimiliano Mirabella; Aldobrando Broccolini
Journal:  J Neurol       Date:  2012-01-10       Impact factor: 4.849

Review 4.  Hereditary inclusion body myopathy: a decade of progress.

Authors:  Marjan Huizing; Donna M Krasnewich
Journal:  Biochim Biophys Acta       Date:  2009-07-24

5.  Prophylactic treatment with sialic acid metabolites precludes the development of the myopathic phenotype in the DMRV-hIBM mouse model.

Authors:  May Christine V Malicdan; Satoru Noguchi; Yukiko K Hayashi; Ikuya Nonaka; Ichizo Nishino
Journal:  Nat Med       Date:  2009-06       Impact factor: 53.440

6.  Prevalence and impact of musculoskeletal injury among endoscopists: a controlled pilot study.

Authors:  Stephanie L Hansel; Michael D Crowell; Darrell S Pardi; Ernest P Bouras; John K DiBaise
Journal:  J Clin Gastroenterol       Date:  2009 May-Jun       Impact factor: 3.062

Review 7.  GNE myopathy: current update and future therapy.

Authors:  Ichizo Nishino; Nuria Carrillo-Carrasco; Zohar Argov
Journal:  J Neurol Neurosurg Psychiatry       Date:  2014-07-07       Impact factor: 10.154

8.  Maximum voluntary isometric contraction: reference values and clinical application.

Authors:  Dara Meldrum; Eibhlis Cahalane; Ronan Conroy; Deirdre Fitzgerald; Orla Hardiman
Journal:  Amyotroph Lateral Scler       Date:  2007-02

9.  Two recurrent mutations are associated with GNE myopathy in the North of Britain.

Authors:  Amina Chaouch; Kathryn M Brennan; Judith Hudson; Cheryl Longman; John McConville; Patrick J Morrison; Maria E Farrugia; Richard Petty; Willie Stewart; Fiona Norwood; Rita Horvath; Patrick F Chinnery; Donald Costigan; John Winer; Tuomo Polvikoski; Estelle Healy; Anna Sarkozy; Teresinha Evangelista; Oksana Pogoryelova; Michelle Eagle; Kate Bushby; Volker Straub; Hanns Lochmüller
Journal:  J Neurol Neurosurg Psychiatry       Date:  2014-04-02       Impact factor: 10.154

Review 10.  Sialic acids as regulators of molecular and cellular interactions.

Authors:  Roland Schauer
Journal:  Curr Opin Struct Biol       Date:  2009-08-19       Impact factor: 6.809

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  9 in total

1.  Quantitative nuclear magnetic resonance imaging detects subclinical changes over 1 year in skeletal muscle of GNE myopathy.

Authors:  Teresa Gidaro; Harmen Reyngoudt; Julien Le Louër; Anthony Behin; Ferial Toumi; Melanie Villeret; Ericky C A Araujo; Pierre-Yves Baudin; Benjamin Marty; Melanie Annoussamy; Jean-Yves Hogrel; Pierre G Carlier; Laurent Servais
Journal:  J Neurol       Date:  2019-10-15       Impact factor: 4.849

2.  GNE missense mutation in recessive familial amyotrophic lateral sclerosis.

Authors:  Çiğdem Köroğlu; Rezzak Yılmaz; Mine Hayriye Sorgun; Seyhun Solakoğlu; Özden Şener
Journal:  Neurogenetics       Date:  2017-10-31       Impact factor: 2.660

3.  ACTA1-myopathy with prominent finger flexor weakness and rimmed vacuoles.

Authors:  Teerin Liewluck; Zhiyv Niu; Steven A Moore; Mohammad Alsharabati; Margherita Milone
Journal:  Neuromuscul Disord       Date:  2019-03-02       Impact factor: 4.296

4.  Relationship between markers of disease activity and progression in skeletal muscle of GNE myopathy patients using quantitative nuclear magnetic resonance imaging and 31P nuclear magnetic resonance spectroscopy.

Authors:  Harmen Reyngoudt; Benjamin Marty; Ericky Caldas de Almeida Araújo; Pierre-Yves Baudin; Julien Le Louër; Jean-Marc Boisserie; Anthony Béhin; Laurent Servais; Teresa Gidaro; Pierre G Carlier
Journal:  Quant Imaging Med Surg       Date:  2020-07

5.  Generation and Characterization of a Skeletal Muscle Cell-Based Model Carrying One Single Gne Allele: Implications in Actin Dynamics.

Authors:  Shamulailatpam Shreedarshanee Devi; Rashmi Yadav; Fluencephila Mashangva; Priyanka Chaudhary; Shweta Sharma; Ranjana Arya
Journal:  Mol Neurobiol       Date:  2021-09-12       Impact factor: 5.590

6.  Clinical and Genomic Evaluation of 207 Genetic Myopathies in the Indian Subcontinent.

Authors:  Samya Chakravorty; Babi Ramesh Reddy Nallamilli; Satish Vasant Khadilkar; Madhu Bala Singla; Ashish Bhutada; Rashna Dastur; Pradnya Satish Gaitonde; Laura E Rufibach; Logan Gloster; Madhuri Hegde
Journal:  Front Neurol       Date:  2020-11-05       Impact factor: 4.086

7.  Gene analysis and clinical features of 22 GNE myopathy patients.

Authors:  Xuan Guo; Zhe Zhao; Hongrui Shen; Qi Bing; Nan Li; Jiannan Chen; Jing Hu
Journal:  Neurol Sci       Date:  2022-04-19       Impact factor: 3.830

Review 8.  GNE Myopathy: Etiology, Diagnosis, and Therapeutic Challenges.

Authors:  Nuria Carrillo; May C Malicdan; Marjan Huizing
Journal:  Neurotherapeutics       Date:  2018-10       Impact factor: 7.620

9.  GNE Myopathy with Prominent Axial Muscle Involvement.

Authors:  Jin Mo Park; Jin Hong Shin; Jin Sung Park
Journal:  J Clin Neurol       Date:  2018-09-06       Impact factor: 3.077

  9 in total

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