Literature DB >> 22431881

Consensus statement on standard of care for congenital myopathies.

Ching H Wang1, James J Dowling, Kathryn North, Mary K Schroth, Thomas Sejersen, Frederic Shapiro, Jonathan Bellini, Hali Weiss, Marc Guillet, Kimberly Amburgey, Susan Apkon, Enrico Bertini, Carsten Bonnemann, Nigel Clarke, Anne M Connolly, Brigitte Estournet-Mathiaud, Dominic Fitzgerald, Julaine M Florence, Richard Gee, Juliana Gurgel-Giannetti, Allan M Glanzman, Brittany Hofmeister, Heinz Jungbluth, Anastassios C Koumbourlis, Nigel G Laing, Marion Main, Leslie A Morrison, Craig Munns, Kristy Rose, Pamela M Schuler, Caroline Sewry, Kari Storhaug, Mariz Vainzof, Nanci Yuan.   

Abstract

Recent progress in scientific research has facilitated accurate genetic and neuropathological diagnosis of congenital myopathies. However, given their relatively low incidence, congenital myopathies remain unfamiliar to the majority of care providers, and the levels of patient care are extremely variable. This consensus statement aims to provide care guidelines for congenital myopathies. The International Standard of Care Committee for Congenital Myopathies worked through frequent e-mail correspondences, periodic conference calls, 2 rounds of online surveys, and a 3-day workshop to achieve a consensus for diagnostic and clinical care recommendations. The committee includes 59 members from 10 medical disciplines. They are organized into 5 working groups: genetics/diagnosis, neurology, pulmonology, gastroenterology/nutrition/speech/oral care, and orthopedics/rehabilitation. In each care area the authors summarize the committee's recommendations for symptom assessments and therapeutic interventions. It is the committee's goal that through these recommendations, patients with congenital myopathies will receive optimal care and improve their disease outcome.

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Year:  2012        PMID: 22431881      PMCID: PMC5234865          DOI: 10.1177/0883073812436605

Source DB:  PubMed          Journal:  J Child Neurol        ISSN: 0883-0738            Impact factor:   1.987


  106 in total

1.  Obstetric aspects in women with facioscapulohumeral muscular dystrophy, limb-girdle muscular dystrophy, and congenital myopathies.

Authors:  S Rudnik-Schöneborn; B Glauner; D Röhrig; K Zerres
Journal:  Arch Neurol       Date:  1997-07

2.  Expanding the clinical, pathological and MRI phenotype of DNM2-related centronuclear myopathy.

Authors:  Rachel D Susman; Susana Quijano-Roy; Nan Yang; Richard Webster; Nigel F Clarke; Jim Dowling; Marina Kennerson; Garth Nicholson; Valerie Biancalana; Biljana Ilkovski; Kevin M Flanigan; Susan Arbuckle; Chandra Malladi; Phillip Robinson; Steven Vucic; Michèle Mayer; Norma B Romero; Jon Andoni Urtizberea; Federico García-Bragado; Pascale Guicheney; Marc Bitoun; Robert-Yves Carlier; Kathryn N North
Journal:  Neuromuscul Disord       Date:  2010-03-12       Impact factor: 4.296

3.  Cardiac manifestations of congenital fiber-type disproportion myopathy.

Authors:  B L Banwell; L E Becker; V Jay; G P Taylor; J Vajsar
Journal:  J Child Neurol       Date:  1999-02       Impact factor: 1.987

4.  Central core disease. Clinical features in 13 patients.

Authors:  A Shuaib; R T Paasuke; K W Brownell
Journal:  Medicine (Baltimore)       Date:  1987-09       Impact factor: 1.889

5.  Myalgia as the revealing symptom of multicore disease and fibre type disproportion myopathy.

Authors:  C Sobreira; W Marques; A A Barreira
Journal:  J Neurol Neurosurg Psychiatry       Date:  2003-09       Impact factor: 10.154

6.  Dietary L-tyrosine supplementation in nemaline myopathy.

Authors:  Monique M Ryan; Catherine Sy; Sian Rudge; Carolyn Ellaway; David Ketteridge; Laurence G Roddick; Susan T Iannaccone; Andrew J Kornberg; Kathryn N North
Journal:  J Child Neurol       Date:  2007-12-13       Impact factor: 1.987

7.  Dentofacial characteristics of growing patients with Duchenne muscular dystrophy: a morphological study.

Authors:  Catherine Morel-Verdebout; Sébastien Botteron; Stavros Kiliaridis
Journal:  Eur J Orthod       Date:  2007-10       Impact factor: 3.075

Review 8.  Muscle disease caused by mutations in the skeletal muscle alpha-actin gene (ACTA1).

Authors:  John C Sparrow; Kristen J Nowak; Hayley J Durling; Alan H Beggs; Carina Wallgren-Pettersson; Norma Romero; Ikuya Nonaka; Nigel G Laing
Journal:  Neuromuscul Disord       Date:  2003-09       Impact factor: 4.296

Review 9.  Centronuclear (myotubular) myopathy.

Authors:  Heinz Jungbluth; Carina Wallgren-Pettersson; Jocelyn Laporte
Journal:  Orphanet J Rare Dis       Date:  2008-09-25       Impact factor: 4.123

Review 10.  Malignant hyperthermia.

Authors:  Henry Rosenberg; Mark Davis; Danielle James; Neil Pollock; Kathryn Stowell
Journal:  Orphanet J Rare Dis       Date:  2007-04-24       Impact factor: 4.123

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  24 in total

1.  Congenital myopathies: Natural history of a large pediatric cohort.

Authors:  Irene Colombo; Mariacristina Scoto; Adnan Y Manzur; Stephanie A Robb; Lorenzo Maggi; Vasantha Gowda; Thomas Cullup; Michael Yau; Rahul Phadke; Caroline Sewry; Heinz Jungbluth; Francesco Muntoni
Journal:  Neurology       Date:  2014-11-26       Impact factor: 9.910

Review 2.  Pulmonary Manifestations of Neuromuscular Diseases.

Authors:  Umakanth Amabalalsa Khatwa; Fei Jamie Dy
Journal:  Indian J Pediatr       Date:  2015-07-23       Impact factor: 1.967

Review 3.  Congenital or Early Developing Neuromuscular Diseases Affecting Feeding, Swallowing and Speech - A Review of the Literature from January 1998 to August 2021.

Authors:  Lotta Sjögreen; Lisa Bengtsson
Journal:  J Neuromuscul Dis       Date:  2022

Review 4.  Multidisciplinary approach to the management of myopathies.

Authors:  Wendy M King; John T Kissel
Journal:  Continuum (Minneap Minn)       Date:  2013-12

5.  An integrated diagnosis strategy for congenital myopathies.

Authors:  Johann Böhm; Nasim Vasli; Edoardo Malfatti; Stéphanie Le Gras; Claire Feger; Bernard Jost; Nicole Monnier; Julie Brocard; Hatice Karasoy; Marion Gérard; Maggie C Walter; Peter Reilich; Valérie Biancalana; Christine Kretz; Nadia Messaddeq; Isabelle Marty; Joël Lunardi; Norma B Romero; Jocelyn Laporte
Journal:  PLoS One       Date:  2013-06-24       Impact factor: 3.240

Review 6.  Congenital myopathies: disorders of excitation-contraction coupling and muscle contraction.

Authors:  Heinz Jungbluth; Susan Treves; Francesco Zorzato; Anna Sarkozy; Julien Ochala; Caroline Sewry; Rahul Phadke; Mathias Gautel; Francesco Muntoni
Journal:  Nat Rev Neurol       Date:  2018-02-02       Impact factor: 42.937

7.  A case of dermatomyositis in a patient with central core disease: unusual association with autoimmunity and genetic muscle disease.

Authors:  Min Jung Kim; Mi Hyeon Kim; Sung-Hye Park; Yeong Wook Song
Journal:  Pediatr Rheumatol Online J       Date:  2021-06-30       Impact factor: 3.054

8.  Profound Hypotonia and Respiratory Failure due to Suspected Nemaline Myopathy in a Preterm Infant.

Authors:  Gloria Akuamoah-Boateng; Raymond C Stetson; Bethany D Kaemingk; David A Bieber; Jane E Brumbaugh
Journal:  AJP Rep       Date:  2021-06-23

9.  Combined MRI and ³¹P-MRS investigations of the ACTA1(H40Y) mouse model of nemaline myopathy show impaired muscle function and altered energy metabolism.

Authors:  Charlotte Gineste; Yann Le Fur; Christophe Vilmen; Arnaud Le Troter; Emilie Pecchi; Patrick J Cozzone; Edna C Hardeman; David Bendahan; Julien Gondin
Journal:  PLoS One       Date:  2013-04-16       Impact factor: 3.240

10.  Multimodal MRI and (31)P-MRS investigations of the ACTA1(Asp286Gly) mouse model of nemaline myopathy provide evidence of impaired in vivo muscle function, altered muscle structure and disturbed energy metabolism.

Authors:  Charlotte Gineste; Guillaume Duhamel; Yann Le Fur; Christophe Vilmen; Patrick J Cozzone; Kristen J Nowak; David Bendahan; Julien Gondin
Journal:  PLoS One       Date:  2013-08-20       Impact factor: 3.240

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