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...

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Detalles Bibliográficos
Autores principales: Pelicano Paulos, Jorge, Artilheiro, Vanessa, Cruz, Catarina, Carneiro, Ana Pinto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Case Reports
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

Internet

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

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