Colombian consensus for the follow-up of patients with Duchenne muscular dystrophy

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Maritza Muñoz Rivas
Sandra Milena Castellar Leones
Edicson Ruiz Ospina
Diego M. Chaustre Ruiz
Rogelio Camacho Echeverri
Maria Eugenia Miño Arango
Blanca Doris Rodríguez
Lina Marcela Tavera Saldaña
Pilar Guerrero
Martha Piñeros
Dagoberto Cabrera Hemer
Juan Carlos Prieto
Asid Rodríguez
Martha Gómez
Carolina Rivera
Marcela Galvez
Gustavo Contreras García
Sandra Ospina
Lina Mora
Lina Moreno
José María Satizábal Soto
Diana Pilar Soto Peña
Manuel Huertas Quiñoñes
Jenny Jurado
Sergio Nossa
Ximena Palacios
Pilar Guarnizo
Luz Helena Castaño
Mary Garcia

Abstract

Duchenne muscular dystrophy (DMD) is the most common myopathy in children, X-linked recessive disease, caused by mutations in the DMD gene (Xp21.2). It is characterized by progressive muscular atrophy and weakness, with consequent musculoskeletal, respiratory and cardiac complications, among others. Considering the high prevalence of this condition (Worldwide prevalence 0.5 per 10,000 men) (1,2) and the importance of multidisciplinary management for the timely diagnosis and proper management of patients, an interdisciplinary consensus of experts is made to propose recommendations for the diagnosis and follow up of Colombian patients with DMD.

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How to Cite
Muñoz Rivas, M. ., Castellar Leones, S. M. ., Ruiz Ospina, E. ., Chaustre Ruiz, D. M. ., Camacho Echeverri, R. ., Miño Arango, M. E., … Garcia, M. (2020). Colombian consensus for the follow-up of patients with Duchenne muscular dystrophy. Pediatría, 52(3), 75–84. https://doi.org/10.14295/p.v52i3.153
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Review topics

References

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