Delay in Diagnosis of Duchenne Muscular Dystrophy

Investigators from Johns Hopkins Hospital, Baltimore, MD, retrospectively reviewed 179 records of patients with Duchenne muscular dystrophy (DMD) evaluated between 1989 and 2012. Diagnosis was confirmed by genetic testing or muscle biopsy, and clinical data were complete in 107 patients.

Detalles Bibliográficos
Autores principales: Rao, Vamshi K., Kuntz, Nancy L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Pediatric Neurology Briefs Publishers 2015
Materias:
Muscle Disorders
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4747303/
https://www.ncbi.nlm.nih.gov/pubmed/26933528
http://dx.doi.org/10.15844/pedneurbriefs-29-1-4
Descripción
Sumario:Investigators from Johns Hopkins Hospital, Baltimore, MD, retrospectively reviewed 179 records of patients with Duchenne muscular dystrophy (DMD) evaluated between 1989 and 2012. Diagnosis was confirmed by genetic testing or muscle biopsy, and clinical data were complete in 107 patients.

Ejemplares similares