TY - JOUR
T1 - Diagnosis and management of spinal muscular atrophy
T2 - Part 1: Recommendations for diagnosis, rehabilitation, orthopedic and nutritional care
AU - SMA Care Group
AU - Mercuri, Eugenio
AU - Finkel, Richard S.
AU - Muntoni, Francesco
AU - Wirth, Brunhilde
AU - Montes, Jacqueline
AU - Main, Marion
AU - Mazzone, Elena S.
AU - Vitale, Michael
AU - Snyder, Brian
AU - Quijano-Roy, Susana
AU - Bertini, Enrico
AU - Davis, Rebecca Hurst
AU - Meyer, Oscar H.
AU - Simonds, Anita K.
AU - Schroth, Mary K.
AU - Graham, Robert J.
AU - Kirschner, Janbernd
AU - Iannaccone, Susan T.
AU - Crawford, Thomas O.
AU - Woods, Simon
AU - Qian, Ying
AU - Sejersen, Thomas
AU - Tiziano, Francesco Danilo
AU - Tizzano, Eduardo
AU - Topaloglu, Haluk
AU - Swoboda, Kathy
AU - Laing, Nigel
AU - Kayoko, Saito
AU - Prior, Thomas
AU - Chung, Wendy K.
AU - Wu, Shou Mei
AU - Coleman, Caron
AU - Gee, Richard
AU - Glanzman, Allan
AU - Kroksmark, Anna Karin
AU - Krosschell, Kristin
AU - Nelson, Leslie
AU - Rose, Kristy
AU - Stępień, Agnieszka
AU - Vuillerot, Carole
AU - Dubousset, Jean
AU - Farrington, David
AU - Flynn, Jack
AU - Halanski, Matthew
AU - Hasler, Carol
AU - Miladi, Lotfi
AU - Reilly, Christopher
AU - Roye, Benjamin
AU - Yazici, Muharrem
AU - Hurst, Rebecca
N1 - Publisher Copyright:
© 2017
PY - 2018/2/1
Y1 - 2018/2/1
N2 - Spinal muscular atrophy (SMA) is a severe neuromuscular disorder due to a defect in the survival motor neuron 1 (SMN1) gene. Its incidence is approximately 1 in 11,000 live births. In 2007, an International Conference on the Standard of Care for SMA published a consensus statement on SMA standard of care that has been widely used throughout the world. Here we report a two-part update of the topics covered in the previous recommendations. In part 1 we present the methods used to achieve these recommendations, and an update on diagnosis, rehabilitation, orthopedic and spinal management; and nutritional, swallowing and gastrointestinal management. Pulmonary management, acute care, other organ involvement, ethical issues, medications, and the impact of new treatments for SMA are discussed in part 2.
AB - Spinal muscular atrophy (SMA) is a severe neuromuscular disorder due to a defect in the survival motor neuron 1 (SMN1) gene. Its incidence is approximately 1 in 11,000 live births. In 2007, an International Conference on the Standard of Care for SMA published a consensus statement on SMA standard of care that has been widely used throughout the world. Here we report a two-part update of the topics covered in the previous recommendations. In part 1 we present the methods used to achieve these recommendations, and an update on diagnosis, rehabilitation, orthopedic and spinal management; and nutritional, swallowing and gastrointestinal management. Pulmonary management, acute care, other organ involvement, ethical issues, medications, and the impact of new treatments for SMA are discussed in part 2.
KW - Care
KW - Diagnosis
KW - Nutrition
KW - Orthopedic
KW - Phisotherapy
KW - Spinal muscular atrophy
UR - http://www.scopus.com/inward/record.url?scp=85044858023&partnerID=8YFLogxK
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U2 - 10.1016/j.nmd.2017.11.005
DO - 10.1016/j.nmd.2017.11.005
M3 - Article
C2 - 29290580
AN - SCOPUS:85044858023
SN - 0960-8966
VL - 28
SP - 103
EP - 115
JO - Neuromuscular Disorders
JF - Neuromuscular Disorders
IS - 2
ER -