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A difficult airway approach in a merosin-deficient congenital muscular dystrophy patient: a case report
Merosin-deficient muscular dystrophy is caused by an autosomal recessive mutation on laminin-..2 gene characterized by severe progressive muscle weakness associated with neuromuscular scoliosis and restrictive lung disease. In this case report, we describe an alternative airway approach performed in...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Elsevier
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10533962/ https://www.ncbi.nlm.nih.gov/pubmed/33895222 http://dx.doi.org/10.1016/j.bjane.2021.03.018 |