| Literature DB >> 22431881 |
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.Entities:
Mesh:
Year: 2012 PMID: 22431881 PMCID: PMC5234865 DOI: 10.1177/0883073812436605
Source DB: PubMed Journal: J Child Neurol ISSN: 0883-0738 Impact factor: 1.987