Artículos de revistas
Consensus Statement on Standard of Care for Congenital Myopathies
Fecha
2012Registro en:
JOURNAL OF CHILD NEUROLOGY, THOUSAND OAKS, v. 27, n. 3, pp. 363-382, MAR, 2012
0883-0738
10.1177/0883073812436605
Autor
Wang, Ching H.
Dowling, James J.
North, Kathryn
Schroth, Mary K.
Sejersen, Thomas
Shapiro, Frederic
Bellini, Jonathan
Weiss, Hali
Guillet, Marc
Amburgey, Kimberly
Apkon, Susan
Bertini, Enrico
Bonnemann, Carsten
Clarke, Nigel
Connolly, Anne M.
Estournet-Mathiaud, Brigitte
Fitzgerald, Dominic
Florence, Julaine M.
Gee, Richard
Gurgel-Giannetti, Juliana
Glanzman, Allan M.
Hofmeister, Brittany
Jungbluth, Heinz
Koumbourlis, Anastassios C.
Laing, Nigel G.
Main, Marion
Morrison, Leslie A.
Munns, Craig
Rose, Kristy
Schuler, Pamela M.
Sewry, Caroline
Storhaug, Kari
Vainzof, Mariz
Yuan, Nanci
Institución
Resumen
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.