Literature DB >> 15564032

Magnetic resonance imaging of muscle in nemaline myopathy.

Heinz Jungbluth1, Caroline A Sewry, Serena Counsell, Joanna Allsop, Arijit Chattopadhyay, Eugenio Mercuri, Kathryn North, Nigel Laing, Graeme Bydder, Katarina Pelin, Carina Wallgren-Pettersson, Francesco Muntoni.   

Abstract

We report muscle MRI findings of 10 patients from 8 families with nemaline myopathy. Patients with involvement of the nebulin (NEB) gene showed a consistent pattern of selective muscle involvement corresponding to clinical severity. In mild cases, there was complete sparing of thigh muscles and selective involvement of tibialis anterior and soleus. In moderate cases, there was predominant involvement of rectus femoris, vastus lateralis and hamstring muscles and diffuse involvement of anterior compartment and soleus. Patients with nemaline myopathy secondary to mutations in the skeletal muscle alpha-actin (ACTA1) gene showed diffuse involvement of thigh and leg muscles with relative sparing of the gastrocnemii. Selective muscle involvement in both genetic categories was distinct from what has been reported in other congenital myopathies. We conclude that muscle MRI may be applied to distinguish nemaline myopathy from other conditions with similar clinical and histopathological features, to supplement clinical assessment in individual patients and to help direct genetic testing.

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Year:  2004        PMID: 15564032     DOI: 10.1016/j.nmd.2004.08.005

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


  20 in total

Review 1.  Magnetic resonance imaging patterns of muscle involvement in genetic muscle diseases: a systematic review.

Authors:  Doris G Leung
Journal:  J Neurol       Date:  2016-11-25       Impact factor: 4.849

Review 2.  Advancements in magnetic resonance imaging-based biomarkers for muscular dystrophy.

Authors:  Doris G Leung
Journal:  Muscle Nerve       Date:  2019-05-14       Impact factor: 3.217

Review 3.  Congenital myopathies: an update.

Authors:  Jessica R Nance; James J Dowling; Elizabeth M Gibbs; Carsten G Bönnemann
Journal:  Curr Neurol Neurosci Rep       Date:  2012-04       Impact factor: 5.081

4.  Dysfunctional sarcomere contractility contributes to muscle weakness in ACTA1-related nemaline myopathy (NEM3).

Authors:  Barbara Joureau; Josine Marieke de Winter; Stefan Conijn; Sylvia J P Bogaards; Igor Kovacevic; Albert Kalganov; Malin Persson; Johan Lindqvist; Ger J M Stienen; Thomas C Irving; Weikang Ma; Michaela Yuen; Nigel F Clarke; Dilson E Rassier; Edoardo Malfatti; Norma B Romero; Alan H Beggs; Coen A C Ottenheijm
Journal:  Ann Neurol       Date:  2018-02-06       Impact factor: 10.422

5.  Sporadic late-onset nemaline myopathy: clinical, pathology and imaging findings in a single center cohort.

Authors:  Mauro Monforte; Guido Primiano; Gabriella Silvestri; Massimiliano Mirabella; Marco Luigetti; Cristina Cuccagna; Enzo Ricci; Serenella Servidei; Giorgio Tasca
Journal:  J Neurol       Date:  2018-01-22       Impact factor: 4.849

6.  Nemaline myopathy type 6: clinical and myopathological features.

Authors:  Montse Olivé; Lev G Goldfarb; Hee-Suk Lee; Zagaa Odgerel; Andre Blokhin; Laura Gonzalez-Mera; Dolores Moreno; Nigel G Laing; Nyamkhishig Sambuughin
Journal:  Muscle Nerve       Date:  2010-12       Impact factor: 3.217

7.  Deleting exon 55 from the nebulin gene induces severe muscle weakness in a mouse model for nemaline myopathy.

Authors:  Coen A C Ottenheijm; Danielle Buck; Josine M de Winter; Claudia Ferrara; Nicoletta Piroddi; Chiara Tesi; Jeffrey R Jasper; Fady I Malik; Hui Meng; Ger J M Stienen; Alan H Beggs; Siegfried Labeit; Corrado Poggesi; Michael W Lawlor; Henk Granzier
Journal:  Brain       Date:  2013-05-28       Impact factor: 13.501

8.  Nebulin (NEB) mutations in a childhood onset distal myopathy with rods and cores uncovered by next generation sequencing.

Authors:  Mariacristina Scoto; Thomas Cullup; Sebahattin Cirak; Shu Yau; Adnan Y Manzur; Lucy Feng; Thomas S Jacques; Glenn Anderson; Stephen Abbs; Caroline Sewry; Heinz Jungbluth; Francesco Muntoni
Journal:  Eur J Hum Genet       Date:  2013-02-27       Impact factor: 4.246

9.  Congenital myopathy caused by a novel missense mutation in the CFL2 gene.

Authors:  C W Ockeloen; H J Gilhuis; R Pfundt; E J Kamsteeg; P B Agrawal; A H Beggs; A Dara Hama-Amin; A Diekstra; N V A M Knoers; M Lammens; N van Alfen
Journal:  Neuromuscul Disord       Date:  2012-05-04       Impact factor: 4.296

10.  In vivo characterization of skeletal muscle function in nebulin-deficient mice.

Authors:  Charlotte Gineste; Augustin C Ogier; Isabelle Varlet; Zaynab Hourani; Monique Bernard; Henk Granzier; David Bendahan; Julien Gondin
Journal:  Muscle Nerve       Date:  2020-01-21       Impact factor: 3.217

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