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Tarjeta de emergencias médicas para la enfermedad de Steinert: una necesidad desatendida
INTRODUCTION. Myotonic dystrophy type 1 (DM1) or Steinert’s disease (ORPHA 273; OMIM #160900) is a rare disorder of genetic origin with muscular manifestations (muscle weakness and myotonia), early-onset cataracts (before 50 years of age) and systemic manifestations (cerebral, endocrine, cardiac, ga...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Viguera Editores (Evidenze Group)
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10364015/ https://www.ncbi.nlm.nih.gov/pubmed/36544372 http://dx.doi.org/10.33588/rn.7601.2022380 |